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105962-47-8

105962-47-8

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105962-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105962-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,6 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105962-47:
(8*1)+(7*0)+(6*5)+(5*9)+(4*6)+(3*2)+(2*4)+(1*7)=128
128 % 10 = 8
So 105962-47-8 is a valid CAS Registry Number.

105962-47-8SDS

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 cis-4-p-chlorophenyl-3-acetamido-3-carbomethoxy-Δ1-pyrazoline

1.2 Other means of identification

Product number -
Other names (3S,4S)-3-Acetylamino-4-(4-chloro-phenyl)-4,5-dihydro-3H-pyrazole-3-carboxylic acid methyl 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:105962-47-8 SDS

105962-47-8Relevant articles and documents

NEW EFFICIENT SYNTHESIS OF 3(5)-CARBOMETHOXY-4-ARYLPYRAZOLES FROM 3-ARYL-2,3-DEHYDROAMINO ACID DERIVATIVES

Catiela, Carlos,Villegas, M. Dolores Diaz de,Gainza, M. Pilar

, p. 165 - 172 (2007/10/02)

3(5)-Carbomethoxy-4-arylpyrazoles can be easily obtained by aromatization with boron trifluoride etherate of 4-aryl-3-acetamido(or benzamido)-3-carbomethoxy-Δ1-pyrazolines synthesized by 1,3-dipolar cycloaddition of diazomethane with 3-aryl-2,3

ON THE SYNTHESIS OF METHYL (Z/E)-2-ACETAMIDO(OR BENZAMIDO)-3-ARYL 2-BUTENOATES

Cativiela, C.,Villegas, M. D. Diaz de,Melendez, E.

, p. 583 - 590 (2007/10/02)

The methyl Z-2-acetamido(or benzamido)-3-aryl-2-butenoates (Z-9a-e, Z-10a-e) were obtained by two alternative procedures: stereospecific opening of Z-2-methyl(or phenyl)-4-(α-arylethylidene)-5(4H)-oxazolones (Z-7a-e, Z-8a-e) and stereospecific homologatio

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