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127903-04-2

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127903-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127903-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,0 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127903-04:
(8*1)+(7*2)+(6*7)+(5*9)+(4*0)+(3*3)+(2*0)+(1*4)=122
122 % 10 = 2
So 127903-04-2 is a valid CAS Registry Number.

127903-04-2SDS

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 N-(4-methoxycarbonylphenyl)sulfuric diamide

1.2 Other means of identification

Product number -
Other names -

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:127903-04-2 SDS

127903-04-2Relevant articles and documents

KINETICS AND MECHANISM OF SOLVOLYSIS OF N-ARYL SULFURIC DIAMIDES

Kavalek, Jaromir,Kralikova, Ulrika,Machacek, Vladimir,Sedlak, Milos,Sterba, Vojeslav

, p. 202 - 222 (2007/10/02)

The methanolysis and hydrolysis kinetics have been studied with the following sulfuric diamide derivatives: N-methyl-N-phenyl- (IIIa), N-methyl-N-(4-methoxycarbonylphenyl)- (IIIb), N-(4-methoxycarbonylphenyl)- (IIIc), N-methyl-N-(2-methoxycarbonylphenyl)- (IIId), N-(2-methoxycarbonylphenyl)- (IIIe), and N-methyl-N-(2,4-dibromophenyl)- (IIIf).The solvolyses of the neutral substrates IIIa and IIIb proceed by the addition-elimination mechanism.In the presence of the solvent lyate ions the solvolyses go by the E1cb mechanism.The solvolyses of the conjugated bases ofcompounds IIIa and IIIb are subject to general acid catalysis, the effects of the ring substituents being opposite to those in the addition-elimination mechanism.The solvolyses of compounds IIId and IIIf exhibit a distinct catalytic effect of neighbouring group; the reaction goes via a reactive intermediate, the transformation of the intermediate into the solvolysis product being subject to general acid and base catalysis.

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