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N-(4-[BENZOYL]BENZYL)-N,N,N-TRIETHYLAMMONIUM BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73603-46-0

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73603-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73603-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,0 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73603-46:
(7*7)+(6*3)+(5*6)+(4*0)+(3*3)+(2*4)+(1*6)=120
120 % 10 = 0
So 73603-46-0 is a valid CAS Registry Number.

73603-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-benzoylphenyl)methyl-triethylazanium,bromide

1.2 Other means of identification

Product number -
Other names N-(4-[BENZOYL]BENZYL)-N,N,N-TRIETHYLAMMONIUM BROMIDE

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:73603-46-0 SDS

73603-46-0Downstream Products

73603-46-0Relevant academic research and scientific papers

Tetraorganylborate salts as convenient precursors for photogeneration of tertiary amines

Sarker, Ananda M.,Lungu, Adrian,Mejiritski, Alexander,Kaneko, Yuji,Neckers, Douglas C.

, p. 2315 - 2331 (2007/10/03)

Photoreactions of p-(benzoyl)benzyl trisubstituted ammonium tetraorganylborate salts for the generation of tertiary amines in solution and rigid matrices are described. Structural modification of the complexes allows study of the influence of steric and electronic effects on the photogeneration of amines. Flash photolysis, cyclic voltammetry and product analysis indicate that single electron transfer from borate to excited benzophenone is followed by homolytic C-N bond cleavage. Photoliberation of the tertiary amine is controlled by the rate of the electron transfer reaction.

UNEXPECTED HIGH PHOTOIXIDIZING EFFICIENCY OF BENZOPHENONE DERIVATIVES HAVING TETRAALKYLAMMONIUM SUBSTITUENTS

Tazuke, Shigeo,Kawasaki, Yasuhiro,Kitamura, Noboru,Inoue, Takashi

, p. 251 - 254 (2007/10/02)

Benzophenone derivatives having various tetraalkylammonium ion in the 4 position (II, III, IV, and V) were found to be much more efficient senzitizers than benzophenone(I) in photooxidation of Leuco Crystal Violet(LCV) to Crystal Violet(CV+) in acetonitrile in air, which was interpreted in terms of the cationic atmosphere effect facilitating the primary electron transfer process from LCV to BP*3.

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