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81053-18-1

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81053-18-1 Usage

General Description

1-Hydroxy-4-oxocyclohexaneacetic acid ethyl ester is a chemical compound with the molecular formula C10H16O4. It is an ester formed from the reaction of ethyl alcohol and 1-hydroxy-4-oxocyclohexaneacetic acid. 1-Hydroxy-4-oxocyclohexaneacetic acid ethyl ester is commonly used in the synthesis of pharmaceuticals and as a building block in organic chemistry. It is also known by the trade name Ethyl 2-oxo-1-cyclohexanecarboxylate. 1-Hydroxy-4-oxocyclohexaneacetic acid ethyl ester is a clear, colorless liquid that is slightly soluble in water but highly soluble in organic solvents such as ethanol and ether. It is commonly used as a reagent in organic synthesis and as a flavoring agent in the food industry.

Check Digit Verification of cas no

The CAS Registry Mumber 81053-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,5 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81053-18:
(7*8)+(6*1)+(5*0)+(4*5)+(3*3)+(2*1)+(1*8)=101
101 % 10 = 1
So 81053-18-1 is a valid CAS Registry Number.

81053-18-1SDS

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 ethyl 2-(1-hydroxy-4-oxocyclohexyl)acetate

1.2 Other means of identification

Product number -
Other names 1-Hydroxy-4-oxocyclohexaneacetic acid ethyl 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:81053-18-1 SDS

81053-18-1Relevant articles and documents

Protection of the carbonyl group as 1,2,4-trioxane and its regeneration under basic conditions

Singh, Chandan,Malik, Heetika

, p. 5673 - 5676 (2007/10/03)

(Chemical Equation Presented) An experimental protocol demonstrating the protection of the carbonyl group as 1,2,4-trioxane, the stability of the protecting group under a variety of reaction conditions, and the regeneration of the carbonyl group with Triton B in THF at room temperature is presented. The method provides a useful alternative for the protection of carbonyl compounds having acid-sensitive moieties.

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