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O,S-dimethyl propylphosphonothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90220-19-2

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90220-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90220-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,2 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90220-19:
(7*9)+(6*0)+(5*2)+(4*2)+(3*0)+(2*1)+(1*9)=92
92 % 10 = 2
So 90220-19-2 is a valid CAS Registry Number.

90220-19-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[methoxy(methylsulfanyl)phosphoryl]propane

1.2 Other means of identification

Product number -
Other names Phosphonothioic acid,propyl-,O,S-dimethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90220-19-2 SDS

90220-19-2Upstream product

90220-19-2Downstream Products

90220-19-2Relevant academic research and scientific papers

Thiophosphonate inhibitors of phosphatase enzymes and metallophosphatases

-

, (2008/06/13)

Compounds of the general formula wherein R is selected from the group consisting essentially of hydrogen, methyl, ethyl, phenyl, a carboxyl, or naphthyl substituted or a carbonyl substituted, alkyl of from 3 to 20 carbon atoms, a mono, bi or tri cyclic aryl or substituted aryl for the inhibition of phosphatase enzymes, including metallophosphatases; and, novel methods for synthesizing such compounds. The methods of use include the administration of an effective amount of the compound to provide effective phosphatase inhibition and therapeutic use to treat or prevent certain diseases, which utilize specific phosphatase enzymes.

Thiophosphonate inhibitors of phosphatase enzymes and metallophosphatases

-

Page/Page column 12, (2010/02/11)

Compounds of the general formula wherein R is selected from the group consisting essentially of hydrogen, methyl, ethyl, phenyl, a carboxyl, or naphthyl substituted or a carbonyl substituted, alkyl of from 3 to 20 carbon atoms, a mono, bi or tri cyclic aryl or substituted aryl for the inhibition of phosphatase enzymes, including metallophosphatases; and, novel methods for synthesizing such compounds. The methods of use include the administration of an effective amount of the compound to provide effective phosphatase inhibition and therapeutic use to treat or prevent certain diseases, which utilize specific phosphatase enzymes.

A convenient synthesis of phosphonothioic acids

Swierczek, Krzysztof,Peters, John W.,Hengge, Alvan C.

, p. 595 - 599 (2007/10/03)

A method for the convenient synthesis of phosphonothioates, or phosphonothioic acids, is reported. A significant advantage of the method is the alleviation of the need for purification of intermediates, other than washing with water. No chromatography is needed and the only purification step is the crystallization of the final product. The method uses standard reagents and should be applicable to the synthesis of phosphonothioic acids bearing a range of functional groups.

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