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N,N'-(methylenedi-4,1-phenylene)bis[dibenzylamine] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69595-64-8

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69595-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69595-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,9 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69595-64:
(7*6)+(6*9)+(5*5)+(4*9)+(3*5)+(2*6)+(1*4)=188
188 % 10 = 8
So 69595-64-8 is a valid CAS Registry Number.

69595-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dibenzyl-4-[[4-(dibenzylamino)phenyl]methyl]aniline

1.2 Other means of identification

Product number -
Other names EINECS 274-054-0

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:69595-64-8 SDS

69595-64-8Downstream Products

69595-64-8Relevant academic research and scientific papers

One-Pot Synthesis of N-Alkyl Benzotriazoles via a Br?nsted Acid-Catalyzed Three-Component Reaction

Wang, Xiangdong,Jia, Chunqi,Feng, Yadong,Wang, Lianhui,Cui, Xiuling

supporting information, p. 374 - 378 (2017/11/16)

A novel three-component condensation reaction of benzotriazoles, aldehydes and tertiary anilines efficiently catalyzed by readily available organic acid p-toluenesulfonic acid (PTSA) has been developed. A series of N-alkyl benzotriazoles were synthesized in up to 97% yield for 21 examples starting from anilines, benzotriazoles and formaldehyde. This strategy features a simple system, atom economy, environmental friendliness, high efficiency, excellent regioselectivity, good functional group tolerance, easily available starting materials, and cheap catalyst. The mechanistic studies indicated that aza quinone methide was probably involved as an intermediate in this transformation. (Figure presented.).

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