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19290-47-2

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19290-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19290-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,9 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19290-47:
(7*1)+(6*9)+(5*2)+(4*9)+(3*0)+(2*4)+(1*7)=122
122 % 10 = 2
So 19290-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O3S/c1-3-12(4-2)11(14)17-10-7-5-9(6-8-10)13(15)16/h5-8H,3-4H2,1-2H3

19290-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(4-nitrophenyl) N,N-diethylcarbamothioate

1.2 Other means of identification

Product number -
Other names Carbamicacid,diethylthio-,S-(p-nitrophenyl) ester (8CI)

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:19290-47-2 SDS

19290-47-2Downstream Products

19290-47-2Relevant articles and documents

A facile method for the synthesis of thiocarbamates: Palladium-catalyzed reaction of disulfide, amine, and carbon monoxide

Nishiyama, Yutaka,Kawamatsu, Hiroaki,Sonoda, Noboru

, p. 2551 - 2554 (2007/10/03)

(Equation Presented) A new method for the synthesis of thiocarbamates has been developed. When dialkyl or diaryl disulfides were allowed to react with secondary amines and carbon monoxide in the presence of a catalytic amount of a palladium complex, the thiocarbamates were obtained in moderate to good yields. In contrast to that of secondary amines, in the reaction of a primary amine, no formation of thiocarbamate was confirmed, but urea was formed in good yield.

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