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N-methyl-N-phenyl-β?enaminone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57466-25-8

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57466-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57466-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,6 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57466-25:
(7*5)+(6*7)+(5*4)+(4*6)+(3*6)+(2*2)+(1*5)=148
148 % 10 = 8
So 57466-25-8 is a valid CAS Registry Number.

57466-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-phenyl-3-amino-2-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names 3-[methyl(phenyl)amino]cyclohex-2-enone

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:57466-25-8 SDS

57466-25-8Relevant academic research and scientific papers

Formation of 3-Aminophenols from Cyclohexane-1,3-diones

Szymor-Pietrzak, Damian,Khan, Muhammad N.,Pagès, Ana?s,Kumar, Ajay,Depner, Noah,Clive, Derrick L. J.

, p. 619 - 631 (2021)

meta-Aminophenols are formed by the action of DBU on 3-amino-2-chlorocyclohex-2-en-1-ones at room temperature in MeCN. The chloro compounds are generated by treating 3-aminocyclohex-2-en-1-ones with the easily prepared halogenating agent BnNMe3·ICl2 in Me

Syntheses of N-alkylated carbazolones via Pd(OAc)2-mediated intramolecular coupling of N-substituted 3-(arylamino)cyclohex-2-enones

Bi, Wenying,Yun, Xiliu,Fan, Yanfeng,Qi, Xiuxiang,Du, Yunfei,Huang, Jianhui

supporting information; experimental part, p. 2899 - 2904 (2011/02/25)

A variety of functionalized N-alkylated carbazolones were prepared via N-alkylation of 3-(arylamino)cyclohex-2-enones followed by an intramolecular oxidative coupling mediated by Pd(OAc)2 under an oxygen atmosphere. This approach adopts an inverted sequence, consisting of the conventional annulation and subsequent N-alkylation. Georg Thieme Verlag Stuttgart - New York.

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