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N-(4-Bromophenyl)-N-phenylbenzenemethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57003-80-2

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57003-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57003-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,0 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57003-80:
(7*5)+(6*7)+(5*0)+(4*0)+(3*3)+(2*8)+(1*0)=102
102 % 10 = 2
So 57003-80-2 is a valid CAS Registry Number.

57003-80-2SDS

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 N-(4-Bromophenyl)-N-phenylbenzenemethanamine

1.2 Other means of identification

Product number -
Other names N-(4-Chlorophenyl)-N-phenyl-benzenemethanamine

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:57003-80-2 SDS

57003-80-2Downstream Products

57003-80-2Relevant academic research and scientific papers

Aromatic tertiary amines, enamines, deoxybenzoins and benzils

-

, (2008/06/13)

A novel synthesis of aromatic tertiary amines involves reacting an aromatic anil and an aromatic ether in a molar ratio of 1:1; adjusting the ratio to 2:1 produces novel enamines and by employing a two step process for enamine production, various unsymmetrically substituted enamines can be obtained which are readily hydrolyzed to corresponding deoxybenzoins which in turn are readily oxidized to benzils, the aromatic tertiary amines may be used to produce charge transport layers in xerography, while the benzils may be used to produce a variety of desired polymers.

Novel Synthesis of N,N-Diarylarylmethanamines from N-(Arylmethylene)arenamines and (Arylmethoxy)arenes

Paventi, Martino,Hay, Allan S.

, p. 5875 - 5882 (2007/10/02)

Various N,N-diarylarylmethanamines were synthesized by the reaction of N-(arylmethylene)arenamines with (arylmethoxy)arenes in dimethylformamide solution in the presence of a strong base as a catalyst which is obtained in situ by reacting metallic sodium with this solvent.In general, the reaction may be depicted as the reduction of the imine and addition, on the original imino nitrogen atom, of the aryl group (of the aryloxy moiety) of the ether and presumably oxidation of the arylmethoxy group of the ether to its corresponding aldehyde.Side reactions and a proposed reaction mechanism are discussed.

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