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20771-77-1

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20771-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20771-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,7 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20771-77:
(7*2)+(6*0)+(5*7)+(4*7)+(3*1)+(2*7)+(1*7)=101
101 % 10 = 1
So 20771-77-1 is a valid CAS Registry Number.

20771-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyanilino)-1-phenylbut-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-<p-Methoxy-anilino>-1-phenyl-but-2-en-1-on

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:20771-77-1 SDS

20771-77-1Relevant articles and documents

Synthesis and characterisation of bis(β-ketoaminato) complexes of cobalt(ii)

Robson, Kiyoshi C. D.,Phillips, Cory D.,Patrick, Brian O.,McNeil, W. Stephen

, p. 2573 - 2578 (2010)

Condensation of 1-phenyl-1,3-butanedione with various substituted anilines affords N-aryl substituted β-ketoamines PhC(O)CHC(CH3)Naryl, which, when deprotonated and reacted with Co(OAc)2·4H 2O yields a series of bis(β-keto

Solid-state synthesis of β-enamino ketones from solid 1,3-dicarbonyl compounds and ammonium salts or amines

Xu, Shi-Liang,Li, Cheng-Ping,Li, Jing-Hua

experimental part, p. 818 - 822 (2009/07/18)

A facile amination of solid 1,3-dicarbonyl compounds with ammonium salts or amines in solid state has been achieved by mechanochemical grinding in the presence of KHSO4 and SiO2. Most of the reactions proceed smoothly at room temperature under solid-state conditions and give their corresponding β-imino derivatives in high yields. The method has the advantage of simple manipulation and mild conditions. Georg Thieme Verlag Stuttgart.

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