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40235-78-7

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40235-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40235-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40235-78:
(7*4)+(6*0)+(5*2)+(4*3)+(3*5)+(2*7)+(1*8)=87
87 % 10 = 7
So 40235-78-7 is a valid CAS Registry Number.

40235-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-thiazolone-5-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl 4-methyl-2-thiazolinone-5-carboxylate

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:40235-78-7 SDS

40235-78-7Relevant articles and documents

AMINOPHENYLCYCLOPROPYL CARBOXYLIC ACIDS AND DERIVATIVES AS AGONISTS TO GPR40

-

Page/Page column 67, (2008/06/13)

The present invention relates generally to novel therapeutic compounds and more particularly to novel compounds, their use as GPR40 agonists, processes for their manufacture, and intermediates useful in their preparation.

Pyrazolecarboxylic acid derivatives and plant disease control agent

-

, (2008/06/13)

The present invention provides a plant disease control agent containing as active ingredient one or more compounds of the formula [1]A--COOR 1 [1]whereinR 1 represents a hydrogen atom or a C 1 -C 4 alkyl group, andA represents a group of the formula (A-1) or (A-2) STR1 R 2 represents a C 1 -C 4 alkyl group, R 3 represents a C 1 -C 4 alkyl group,R 4 represents a halogen atom or a C 1 -C 4 alkyl group, andR 5 represents a C 1 -C 4 alkyl group.Further, the compound of A-1 in the formula [1] in which R 3 is a halogen atom is also included in the present invention.

Synthesis of Heterocyclic Compounds from 0-Aminobenzenethiol and Ammonium Thiocarbamate

D'Amico, John J.,Fuhrhop, Ralph W.,Bollinger, Frederic G.,Dahl, William E.

, p. 641 - 645 (2007/10/02)

The reaction of o-aminobenzenethiol with carbonyl sulfide in the presence of triethylamine afforded an alternate route for the synthesis of 2-benzothiazolinone (1) in 97-98percent yield.The reaction of ammonium thiocarbamate (2) with 2-chlorocyclohexanone furnished the novel 4,5,6,7-tetrahydro-2-benzothiazolinone (3). 3-Ethoxy-2H-1,4-benzothiazin-2-one (7) was prepared by the reaction of o-aminobenzenethiol with diethyl oxalate.Possible pathways and supporting nmr, ir and mass spectra are discussed.

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