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Phenol, 4-(phenylazo)-, benzoate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16513-94-3

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16513-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16513-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16513-94:
(7*1)+(6*6)+(5*5)+(4*1)+(3*3)+(2*9)+(1*4)=103
103 % 10 = 3
So 16513-94-3 is a valid CAS Registry Number.

16513-94-3SDS

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 4-(phenyldiazenyl)phenyl benzoate

1.2 Other means of identification

Product number -
Other names Phenol, 4-(phenylazo)-, benzoate (ester)

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:16513-94-3 SDS

16513-94-3Relevant academic research and scientific papers

Synergistic effect in the catalysis by pyridine N-oxide-triethylamine mixture of acyl transfer processes with participation of benzoyl, diethoxyphosphinoyl, and p-toluenesulfonyl chlorides

Belousova,Savelova,Simanenko,Panchenko

, p. 111 - 114 (2007/10/03)

The kinetics of benzoylation of substituted phenols with benzoyl chloride in the presence of pyridine N-oxide-triethylamine was analyzed with regard to previously reported data on benzoylation, phosphorylation, and sulfonylation of phenols and carboxylic acids. A common mechanism of the synergistic effect was established. The synergistic effect decreases in the series PhCOCl (EtO)2POCl > TsCl.

Mechanism of catalysis with triethylamine of phenols benzoylation in dioxane. New quality experiment

Belousova,Simanenko,Savelova,Suprun

, p. 1656 - 1664 (2007/10/03)

Acylation kinetics with benzoyl chloride in the presence of triethylamine in dioxane at 25°C was studied for substituted nitrophenols (R = 2,4,6-(NO2)3, 2,5-(NO2)2, 2,4-(NO2)2, 4-NO2/

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