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91012-60-1

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91012-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91012-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,1 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91012-60:
(7*9)+(6*1)+(5*0)+(4*1)+(3*2)+(2*6)+(1*0)=91
91 % 10 = 1
So 91012-60-1 is a valid CAS Registry Number.

91012-60-1SDS

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 Ethanone, 1-(4-hydroxy-3-methoxyphenyl)-2-(methylamino)-

1.2 Other means of identification

Product number -
Other names Acetophenone, 4'-hydroxy-3'-methoxy-2-(methylamino)-

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:91012-60-1 SDS

91012-60-1Downstream Products

91012-60-1Relevant articles and documents

SYNTHESIS OF 3-O-METHYLATED DERIVATIVES OF CATECHOLAMINES

Kulikov, S. V.,Samartsev, M. A.

, p. 280 - 288 (2007/10/02)

3-O-Methylated catecholamines, used in the radioenzyme method for the analysis of catecholamines in blood, were synthesized. The optimum conditions for the production of both the intermediate and the final products were determined. By the use of tetrabutylammonium bromide in the condensation of nitromethane with O-benzylvanilin it is possible to obtain a high yield of 1-(3-methoxy-4-benzyloxyphenyl)-2-nitroethanol. The latter is easily transformed at a palladium catalyst into methylnoradrenaline by reduction with ammonium formate. The reduction of 1-(3-methoxy-4-benzyloxyphenyl)-2-nitroethylene with hydrogen or its donors at a palladium catalyst takes place significantly more readily in the presence of ferric chloride.

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