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3-Ethyl-2-hydroxybenzoic acid is an organic compound with the chemical formula C9H10O3. It is a derivative of benzoic acid, featuring a hydroxyl group at the 2-position and an ethyl group at the 3-position. This white crystalline solid is soluble in water and has a molecular weight of 166.18 g/mol. It is commonly used in the synthesis of pharmaceuticals, dyes, and other organic compounds due to its versatile chemical structure. The compound is also known for its potential applications in the field of materials science, particularly in the development of polymers and coatings.

4295-51-6

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4295-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4295-51-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4295-51:
(6*4)+(5*2)+(4*9)+(3*5)+(2*5)+(1*1)=96
96 % 10 = 6
So 4295-51-6 is a valid CAS Registry Number.

4295-51-6SDS

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 3-ethyl-2-hydroxybenzoic acid

1.2 Other means of identification

Product number -
Other names 3-ethylsalicylic acid

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:4295-51-6 SDS

4295-51-6Relevant academic research and scientific papers

Carboxylation of Phenols with CO2 at Atmospheric Pressure

Luo, Junfei,Preciado, Sara,Xie, Pan,Larrosa, Igor

supporting information, p. 6798 - 6802 (2016/05/11)

A convenient and efficient method for the ortho-carboxylation of phenols under atmospheric CO2 pressure has been developed. This method provides an alternative to the previously reported Kolbe-Schmitt method, which requires very high pressures of CO2. The addition of a trisubstituted phenol has proved essential for the successful carboxylation of phenols with CO2 at standard atmospheric pressure, allowing the efficient preparation of a broad variety of salicylic acids.

External preparation for skin

-

, (2008/06/13)

An external preparing for skin comprising one or more than two types of 2-hydroxy benzoic acid derivative and/or salt thereof represented by the following formula: STR1 wherein R is an alkoxy group or alkyl group in the formula. The external preparation for the skin according to the present invention has a suppression effect on melanine generation by inhibition of tyrosinase activity. Accordingly, an excellent bleaching effect based upon the suppression of chromatosis and a high degree of safety can be obtained.

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