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4-nonylphenyl benzoate is a synthetic chemical compound with the molecular formula C25H26O2. It is an ester derived from 4-nonylphenol and benzoic acid, featuring a benzoate group attached to a nonylphenol moiety. 4-nonylphenyl benzoate is primarily used as a plasticizer, a substance added to plastics to increase their flexibility and workability. It is also employed as a solvent and in the formulation of various industrial products, such as adhesives, sealants, and coatings. Due to its potential environmental and health concerns, the use of 4-nonylphenyl benzoate has been restricted in some regions to minimize its impact on aquatic ecosystems and human health.

6316-62-7

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6316-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6316-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6316-62:
(6*6)+(5*3)+(4*1)+(3*6)+(2*6)+(1*2)=87
87 % 10 = 7
So 6316-62-7 is a valid CAS Registry Number.

6316-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nonylphenyl) benzoate

1.2 Other means of identification

Product number -
Other names 4-nonyllphenyl benzoate

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:6316-62-7 SDS

6316-62-7Downstream Products

6316-62-7Relevant academic research and scientific papers

Metal-free synthesis of aryl esters by coupling aryl carboxylic acids and aryl boronic acids

Ruso, Jayaraman Sembian,Rajendiran, Nagappan,Kumaran, Rajendran Senthil

supporting information, p. 2345 - 2347 (2014/05/06)

A facile synthesis of aryl esters is developed by coupling aryl carboxylic acids and aryl boronic acids in the presence of PhI(OAc)2 and carbonyl diimidazole. A wide range of functional groups were tolerant to the metal-free reaction condition that led to the desired products in good yields.

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