6363 College Blvd Ste 400, Shawnee Mission, KS 66211
Christopher Larson President
Lynne Larson, Inc. Business Services
260 W 52Nd St Apt 14G, New York, NY 10019
Christopher Larson Senior Systems Analyst
Nyu Langone Medical Center General Medical and Surgical Hospitals
550 1St Ave, New York, NY 10016
Christopher Larson Senior Manager Ecommerce
National Basketball Association, Inc. Professional Sports Clubs and Promoters
645 5Th Ave Fl 10, New York, NY 10022
Christopher Larson Manager
G O M LLC
271 Madison Ave SUITE 1100, New York, NY 10016 271 Madison Ave Suite 110 SUITE 1100, New York, NY 10016 195 Brooklawn Ave, Bridgeport, CT 06604 350 Edward St, Fairfield, CT 06824
Christopher Larson Chief Operating Officer, Other Other, President
LYNNE LARSON, INC Apparel Accessories and Cosmetics
PO Box 6650, New York, NY 10150 150 Goodale Rd, Newton, NJ 07860 260 W 52 St, New York, NY 10019 2123151101
Christopher N Larson President,Chairman
LARSON MARITIME, INC
Us Patents
Moving A Financial Account From One Enterprise To Another
Richard Louis Knafelz - Charlotte NC, US David Bowman Jones - , US John DeZervos - Morresville NC, US Robin Griffen Cobb - Virginia Beach VA, US Christopher A. Larson - New York NY, US
Assignee:
Bank of America Corporation - Charlotte NC
International Classification:
G06Q 40/00
US Classification:
705 35
Abstract:
According to some embodiments, a system includes an interface and one or more processors. The interface receives a request from a user to move a first account associated with a first enterprise to a second enterprise where the user has at least one account. The processor(s) determine first configuration settings associated with the first account. The processor(s) create a second account at the second enterprise, select second configuration settings based on the first configuration settings, and apply the second configuration settings to the second account.
Flucarbazone Sodium Hemihydrate Method And Composition
- Cary NC, US Christopher L. Larson - Cary NC, US Cameron Seath Gibb - Apex NC, US
International Classification:
A01N 43/653 A01N 25/04 A01N 41/06 A01N 47/38
Abstract:
A flucarbazone sodium hemihydrate method and composition. A method of suppressing growth of grass and broadleaf weeds is described including applying to said weeds at least one dust-free composition comprising flucarbazone sodium-hemihydrate as an active ingredient. A method for preparing flucarbazone sodium-hemihydrate is also described including treating 4,5-dihydro-3-methoxy-4-methyl-5-oxo-N-[[2-(trifluoromethoxy)phenyl]sulfonyl]-1H-1,2,4-triazole-1-carboxamide (MSU) with aqueous sodium hydroxide under pH-controlled conditions; and confirming that a hemihydrate flucarbazone sodium has been obtained.
Process For Preparation Of O,O Dimethyl Phosphoramidothioate And N-(Methoxymethylsulfanylphosphoryl) Acetamide
- Cary NC, US David HUANG - KUNSHAN, CN Kamal KATARIA - Maharashtra, IN Christopher Lynn LARSON - Cary NC, US Cameron Seath GIBB - Apex NC, US Stephen CORNES - American Canyon CA, US
International Classification:
C07F 9/24
Abstract:
Preparation of O,O-dimethyl phosphoramidothioate and O,O-dimethyl phosphoroamidothioate. A process of making O,O-dimethyl phosphoroamidothioate is described including reacting sulfur with PClto form PSCl, reacting the PSClformed with methanol to form O-methyl phosphorodichloridothioate, and reacting the O-methyl phosphorodichloridothioate formed with methyl lye to form O,O-dimethyl phosphorochloridothioate in solution in CHCl, and reacting the O,O-dimethyl phosphorochloridothioate formed with sodium hydroxide and ammonium hydroxide to form O,O-dimethyl phosphoroamidothioate in solution in CHCl. Reacting the O,O-dimethyl phosphoroamidothioate formed with catalytic dimethyl sulfate to form methamidophos and reacting the methamidophos formed with acetic anhydride to form N-(methoxy-methylsulfanylphosphoryl) acetamide is also described. Throughout the process, the O,O-dimethyl phosphorochloridothioate and the O,O-dimethyl phosphoroamidothioate formed are maintained in solution in CHClat all times.
Manufacturing Method For And Insecticidal Compositions Comprising Thiocyclam Hydrochloride
- Cary NC, US Christopher L. Larson - Cary NC, US Mark T. Singleton - Morris CT, US Kamal L. Kataria - Maharashtra State, IN Samantha Besse - Daban, FR Thomas C. Lovelace - Apex NC, US Chandra S. Kanugala - Telangana, IN Srinivas Vollala - Telangana, IN Balraju Vadla - Telangana, IN
International Classification:
C07D 341/00 A01N 43/32 A01N 43/80
Abstract:
A method for manufacturing an insecticidal compound and insecticidal compositions comprising the insecticidal compound and methods of use are presented herein. The manufacturing method presented herein allows for a high purity grade of thiocyclam hydrochloride to be synthesized. The insecticidal compositions comprising the thiocyclam hydrochloride can be used for prevention of crop destruction by insects. The use of thiocyclam hydrochloride in insecticidal compositions as described herein can achieve greater efficacy than previously known insecticides, by eliminating the insect pests more reliably and efficiently.
Manufacturing Method For And Insecticidal Compositions Comprising Thiocyclam Hydrochloride
- Cary NC, US Christopher L. Larson - Cary NC, US Mark T. Singleton - Morris CT, US Kamal L. Kataria - Maharashtra State, IN Samantha Besse - Daban, FR Thomas C. Lovelace - Apex NC, US Chandra S. Kanugala - Telangana, IN Srinivas Vollala - Telangana, IN Balraju Vadla - Telangana, IN
International Classification:
C07D 341/00 A01N 43/32 A01N 43/80
Abstract:
A method for manufacturing an insecticidal compound and insecticidal compositions comprising the insecticidal compound and methods of use are presented herein. The manufacturing method presented herein allows for a high purity grade of thiocyclam hydrochloride to be synthesized. The insecticidal compositions comprising the thiocyclam hydrochloride can be used for prevention of crop destruction by insects. The use of thiocyclam hydrochloride in insecticidal compositions as described herein can achieve greater efficacy than previously known insecticides, by eliminating the insect pests more reliably and efficiently.
Process For Preparation Of O, O-Dimehyl Phosphoramidothioate And N-(Methoxy-Methylsulfanylphosphoryl) Acetamide
- Cary NC, US David HUANG - Kunshan, CN Kamal KATARIA - Maharashtra, IN Christopher Lynn LARSON - Cary NC, US Cameron Seath GIBB - Apex NC, US Stephen CORNES - American Canyon CA, US
Assignee:
Arysta LifeScience Inc. - Cary NC
International Classification:
C07F 9/24
Abstract:
Preparation of O,O-dimethyl phosphoramidothioate and O,O-dimethyl phosphoroamidothioate. A process of making O,O-dimethyl phosphoroamidothioate is described including reacting sulfur with PClto form PSCl, reacting the PSClformed with methanol to form O-methyl phosphorodichloridothioate, and reacting the O-methyl phosphorodichloridothioate formed with methyl lye to form O,O-dimethyl phosphorochloridothioate in solution in CHCl, and reacting the O,O-dimethyl phosphorochloridothioate formed with sodium hydroxide and ammonium hydroxide to form O,O-dimethyl phosphoroamidothioate in solution in CHCl. Reacting the O,O-dimethyl phosphoroamidothioate formed with catalytic dimethyl sulfate to form methamidophos, and reacting the methamidophos formed with acetic anhydride to form N-(methoxy-methylsulfanylphosphoryl) acetamide is also described. Throughout the process, the O,O-dimethyl phosphorochloridothioate and the O,O-dimethyl phosphoroamidothioate formed are maintained in solution in CHClat all times.
Process For Preparing (E)-(5,6-Dihydro-1,4,2-Dioxazine-3-Yl) (2-Hydroxyphenyl) Methanone O-Methyl Oxime
- Tokyo, JP Cameron Gibb - Apex NC, US Christopher Lynn Larson - Cary NC, US A. Sai Srikanth - Chandrashakar Nagar, Kurnool-2, IN Jivan Dhanraj Pawar - Bangalore, IN Sankar Balakrishnan - Tamilnadu, IN K. N. Ravikumar - Bangalore, IN Avinash Shesharo Mane - Bangalore, IN Sagi Sateesh - Andhra Pradesh, IN Sampadarao Ananda Rao - Andhra Pradesh, IN
International Classification:
C07D 273/01 C07D 413/12
Abstract:
A process for preparing (E)-(5,6-dihydro-1,4,2-dioxazin-3-yl)(2-hydroxyphenyl)methanone O-methyl oxime is described which includes: (i) reacting benzofuran-3(2H)-one O-methyl oxime (1) with at least one nitrite selected from n-butyl nitrite and tert-butyl nitrite, in the presence of a metal alkoxide to form (2Z,32)-2,3-benzofuran-dione O3-methyl dioxime (2) as the predominant isomer; (ii) reacting the (2Z,3Z)-2,3-benzofuran-dione O-methyl dioxime (2) with 2-haloethanol to form (2Z,3Z)-benzofuran-2,3-dione 02-(2-hydroxyethyl) O3-methyl dioxime (3); and (iii) reacting the (2Z,3Z)-benzofuran-2,3-dione 02-(2-hydroxyethyl) & -methyl dioxime (3) with an acid to form (E)-(5,6-dihydro-1,4,2-dioxazin-3-yl)(2-hydroxyphenyl)methanone (9-methyl oxime (4);
Manufacturing Method For And Insecticidal Compositions Comprising Thiocyclam Hydrochloride
- Cary NC, US Christopher L. Larson - Cary NC, US Mark T. Singleton - Morris CT, US Kamal L. Kataria - Maharashtra State, IN Samantha Besse - Daban, FR Thomas C. Lovelace - Apex NC, US Chandra S. Kanugala - Telangana, IN Srinivas Vollala - Telangana, IN Balraju Vadla - Telangana, IN
International Classification:
C07D 341/00 A01N 43/32 A01N 43/80
Abstract:
A method for manufacturing an insecticidal compound and insecticidal compositions comprising the insecticidal compound and methods of use are presented herein. The manufacturing method presented herein allows for a high purity grade of thiocyclam hydrochloride to be synthesized. The insecticidal compositions comprising the thiocyclam hydrochloride can be used for prevention of crop destruction by insects. The use of thiocyclam hydrochloride in insecticidal compositions as described herein can achieve greater efficacy than previously known insecticides, by eliminating the insect pests more reliably and efficiently.
The Cobalt Group Seattle, WA Nov 2012 to Aug 2013 Web/Graphic DesignerFluke Networks Everett, WA Mar 2012 to Nov 2012 Web DesignerThe Cobalt Group Seattle, WA Aug 2010 to Mar 2012 Web/Graphic DesignerBig Blue Meenie Jersey City, NJ Jul 2009 to Jul 2010 Audio Engineer InternshipThe Cobalt Group Seattle, WA Jul 2007 to Jul 2009 Web/Graphic DesignerFirefly Audio Kent, WA Jan 2004 to Jan 2009 Audio EngineerAuBeta Networks, Inc Seattle, WA Nov 2000 to Jun 2007 Provisioning Analyst
Education:
University of Washington Seattle, WA 2002 to 2002 Audio Engineering in Audio
Avera Surgical Associates 310 S Pennsylvania St STE 201, Aberdeen, SD 57401 6052291367 (phone), 6052291002 (fax)
Education:
Medical School University of South Dakota Sanford School of Medicine Graduated: 2003
Procedures:
Appendectomy Bariatric Surgery Colonoscopy Destruction of Lesions on the Anus Esophageal Dilatation Gallbladder Removal Laparoscopic Appendectomy Sigmoidoscopy Thoracoscopy Thyroid Gland Removal Upper Gastrointestinal Endoscopy Breast Biopsy Hemorrhoid Procedures Hernia Repair Laparoscopic Gallbladder Removal Mastectomy Oophorectomy Peripheral Vascular Bypass Pilonidal Cyst Excision Proctosigmoidoscopy Small Bowel Resection Spleen Surgey Varicose Vein Procedures Vasectomy
Conditions:
Abdominal Hernia Appendicitis Breast Disorders Cholelethiasis or Cholecystitis Femoral Hernia
Languages:
English
Description:
Dr. Larson graduated from the University of South Dakota Sanford School of Medicine in 2003. He works in Aberdeen, SD and specializes in General Surgery and Thoracic Surgery. Dr. Larson is affiliated with Avera St Lukes Hospital, Community Memorial Hospital and Dakota Plains Surgical Center.
Dr. Larson graduated from the University of Iowa Carver College of Medicine in 1978. He works in De Pere, WI and specializes in Psychiatry and Child & Adolescent Psychiatry. Dr. Larson is affiliated with Bellin Psychiatric Center.
Dr. Larson graduated from the University of California, Los Angeles David Geffen School of Medicine in 1990. He works in Fresno, CA and specializes in Ophthalmology. Dr. Larson is affiliated with Saint Agnes Medical Center.
Dr. Larson graduated from the University of Wisconsin Medical School in 1975. He works in Sheboygan, WI and 1 other location and specializes in Ophthalmology. Dr. Larson is affiliated with Hospital Sisters Health System St Nicholas Hospital.
Urology PC 5500 Pne Lk Rd, Lincoln, NE 68516 4024898888 (phone), 4024211945 (fax)
Urology Surgical Center 5500 Pne Lk Rd, Lincoln, NE 68516 4024218899 (phone), 4024211945 (fax)
Education:
Medical School University of Nebraska College of Medicine Graduated: 1994
Procedures:
Circumcision Cystourethroscopy Cystoscopy Kidney Stone Lithotripsy Nephrectomy Prostate Biopsy Transurethral Resection of Prostate Urinary Flow Tests Vaginal Repair Vasectomy
Conditions:
Benign Prostatic Hypertrophy Bladder Cancer Calculus of the Urinary System Erectile Dysfunction (ED) Kidney Cancer
Languages:
English
Description:
Dr. Larson graduated from the University of Nebraska College of Medicine in 1994. He works in Lincoln, NE and 1 other location and specializes in Urology. Dr. Larson is affiliated with Bryan Medical Center, Bryan Medical Center West Campus and CHI Health St Elizabeth Medical Center.
Gundersen Lutheran ClinicGundersen Health Systems 3111 Gundersen Dr, Onalaska, WI 54650 6087758100 (phone), 6087754706 (fax)
Gundersen Lutheran ClinicGundersen Health System 1900 South Ave, La Crosse, WI 54601 6087827300 (phone), 6087754429 (fax)
Languages:
English
Description:
Mr. Larson works in Onalaska, WI and 1 other location and specializes in Bariatrician and General Surgery. Mr. Larson is affiliated with Gundersen Health System.
Nelson Elementary School Columbia Heights MN 1971-1977, Inlet View Elementary School Anchorage AK 1977-1978, Central Junior High School Anchorage AK 1978-1980, Central Middle School Columbia Heights MN 1980-1981