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34013-89-3

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34013-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34013-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,1 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34013-89:
(7*3)+(6*4)+(5*0)+(4*1)+(3*3)+(2*8)+(1*9)=83
83 % 10 = 3
So 34013-89-3 is a valid CAS Registry Number.

34013-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-diethoxyphosphorylsulfanyl-N-methylacetamide

1.2 Other means of identification

Product number -
Other names O,O-diethyl S-methyl-carbamoylmethyl phosphorothioate

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:34013-89-3 SDS

34013-89-3Downstream Products

34013-89-3Relevant articles and documents

Cs2CO3-Catalyzed Aerobic Oxidative Cross-Dehydrogenative Coupling of Thiols with Phosphonates and Arenes

Song, Song,Zhang, Yiqun,Yeerlan, Adeli,Zhu, Bencong,Liu, Jianzhong,Jiao, Ning

supporting information, p. 2487 - 2491 (2017/02/23)

An efficient Cs2CO3-catalyzed oxidative coupling of thiols with phosphonates and arenes that uses molecular oxygen as the oxidant is described. These reactions provide not only a novel alkali metal salt catalyzed aerobic oxidation, but also an efficient approach to thiophosphates and sulfenylarenes, which are ubiquitously found in pharmaceuticals and pesticides. The reaction proceeds under simple and mild reaction conditions, tolerates a wide range of functional groups, and is applicable to the late-stage synthesis and modification of bioactive molecules.

2-Chloro-2,4-dioxo-3-methyl-1,3,2-thiazaphospholidine. Comments on its phosphorylating properties

Modro, Agnes M.,Modro, Tomasz A.

, p. 2552 - 2554 (2007/10/02)

2-Alkoxy-2,4-dioxo-3-methyl-1,3,2-thiazaphospholidines undergo facile ring-opening reactions with chloride ion, and, in particular, with water.This reactivity may limit their value as first intermediates in the sequential synthesis of phosphoric diesters from the parent 2-chloro-2,4-dioxo-3-methyl-1,3,2-thiazaphospholidine.

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