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114050-46-3

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114050-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114050-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114050-46:
(8*1)+(7*1)+(6*4)+(5*0)+(4*5)+(3*0)+(2*4)+(1*6)=73
73 % 10 = 3
So 114050-46-3 is a valid CAS Registry Number.

114050-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methoxybenzoyloxy)-pyridine-2(1H)-thione

1.2 Other means of identification

Product number -
Other names .4-methoxy-benzoic acid 2-thioxo-2H-pyridin-1-yl 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:114050-46-3 SDS

114050-46-3Relevant articles and documents

Exploratory Studies of the Photochemistry of N-Hydroxypyridine-2-thione Esters. Generation of Excited Radicals by Laser Flash Photolysis and in a Conventional Fluorescence Spectrometer

Bohne, C.,Boch, R.,Scaiano, J. C.

, p. 5414 - 5418 (2007/10/02)

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THE INVENTION OF RADICAL REACTIONS. PART XV. SOME MECHANISTIC ASPECTS OF THE DECARBOXYLATIVE REARRANGEMENT OF THIOHYDROXAMIC ESTERS

Barton, Derek H. R.,Bridon, Dominique,Fernandez-Picot, Isabel,Zard, Samir Z.

, p. 2733 - 2740 (2007/10/02)

Esters (mixed anhydrides) derived from aliphatic or alicyclic carboxylic acids (RCO2H) and thiohydroxamic acids 2 or 3 undergo a thermally or photochemically induced radical chain reaction to give sulphides 4 with loss of carbon dioxide.On irradiation at low temperature however, the chain reaction is essentially suppressed.Under these conditions moderate to good yields of dimers R-R are obtained from primary acids.The mechanistic and synthetic implications of these observations are discussed.

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