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Methyl 2-(1-hydroxycyclohexyl)-2-phenyl-acetate is a complex organic compound with the molecular formula C16H20O3. It is a derivative of phenylacetic acid, featuring a cyclohexane ring with a hydroxyl group and a phenyl group attached to the acetate moiety. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural properties. It is typically synthesized through a series of chemical reactions involving cyclohexanone, phenylacetic acid, and methyl esterification. The compound's structure and reactivity make it a valuable intermediate in the preparation of certain drugs and other specialty chemicals.

5457-12-5

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5457-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5457-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5457-12:
(6*5)+(5*4)+(4*5)+(3*7)+(2*1)+(1*2)=95
95 % 10 = 5
So 5457-12-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-18-14(16)13(12-8-4-2-5-9-12)15(17)10-6-3-7-11-15/h2,4-5,8-9,13,17H,3,6-7,10-11H2,1H3

5457-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(1-hydroxycyclohexyl)-2-phenyl-acetate

1.2 Other means of identification

Product number -
Other names (1-Hydroxy-cyclohexyl)-phenyl-essigsaeure-methylester

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:5457-12-5 SDS

5457-12-5Downstream Products

5457-12-5Relevant academic research and scientific papers

Electrochemical activation of zinc in the coupling reaction of α-bromoesters with carbonyl compounds

Rollin, Y.,Gebehenne, C.,Derien, S.,Dunach, E.,Perichon, J.

, p. 9 - 14 (1993)

The Reformatsky reaction has been examined using a mild and effective method of electrochemical zinc activation, based on the cathodic reduction of a catalytic amount of zing bromide in acetonitrile.

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