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18005-40-8

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18005-40-8 Usage

Uses

Precursor to chemical warfare agents.

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 148, 1959 DOI: 10.1021/ja01510a034

Check Digit Verification of cas no

The CAS Registry Mumber 18005-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18005-40:
(7*1)+(6*8)+(5*0)+(4*0)+(3*5)+(2*4)+(1*0)=78
78 % 10 = 8
So 18005-40-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H9O2PS/c1-3-5-6(2,4)7/h3H2,1-2H3,(H,4,7)

18005-40-8 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (445037)  O-Ethylmethylphosphonothioate  90%

  • 18005-40-8

  • 445037-1G

  • 4,744.35CNY

  • Detail

18005-40-8SDS

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 ethoxy-hydroxy-methyl-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names EMPSH

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:18005-40-8 SDS

18005-40-8Relevant articles and documents

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Pelchowicz,Z.,Leader,H.

, p. 3320 - 3323 (1963)

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Synthesis method of synthetic intermediate methyl phosphite monoester of glufosinate ammonium

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Paragraph 0065; 0066, (2018/09/08)

The invention belongs to the technical field of synthesis of glufosinate ammonium and in particular relates to a synthesis method of a synthetic intermediate methyl phosphite monoester of glufosinateammonium. Aiming at the common problem of an existing methyl phosphite monoester synthesis method that the cost is too high so that the existing methyl phosphite monoester synthesis method is not applicable to large-scale industrial production, the synthesis method provided by the technical scheme comprises the following steps: [1], enabling methylphosphonothioic dichloride to react with a hydroxyl compound under the action of an alkali A, so as to obtain diethyl methylphosphonothionate; [2], dissolving the diethyl methylphosphonothionate into a solvent B to prepare a diethyl methylphosphonothionate solution; carrying out hydrolysis reaction under the action of an alkali B to generate methylphosphonothioic monoester; [3], dissolving the methylphosphonothioic monoester into a solvent C to prepare a methylphosphonothioic monoester solution; carrying out desulfurization reaction on the methylphosphonothioic monoester solution under the action of a catalyst to prepare the methyl phosphitemonoester. The synthesis method provided by the invention is applicable to a glufosinate ammonium synthesis industry.

SYNTHESIS, REACTION WITH ESTERASES, AND TOXICITY OF O-ALKYL S-(CARBALKOXYMETHYLMERCAPTO)METHYL METHYLTHIOPHOSPHONATES

Mastryukova, T. A.,Shipov, A. E.,Emkuzheva, Z. K.,Brestkin, A. P.,Brik, I. L.,et al.

, p. 838 - 842 (2007/10/02)

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