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2-methylcyclohexyl 3-oxobutanoate is an organic compound with the molecular formula C11H18O3. It is a derivative of cyclohexane, featuring a methyl group attached to the cyclohexane ring and a 3-oxobutanoate (also known as 3-oxobutyrate) group attached to the cyclohexane ring. The 3-oxobutanoate group consists of a four-carbon chain with a carbonyl group (C=O) at the third position and a carboxylate group (-COO-) at the end. 2-methylcyclohexyl 3-oxobutanoate is a colorless liquid with a fruity, floral odor and is used in the fragrance industry as a fixative and in the synthesis of various chemicals. It is also known for its potential use as a biofuel additive and as a precursor in the production of pharmaceuticals and agrochemicals.

6624-87-9

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6624-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6624-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6624-87:
(6*6)+(5*6)+(4*2)+(3*4)+(2*8)+(1*7)=109
109 % 10 = 9
So 6624-87-9 is a valid CAS Registry Number.

6624-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylcyclohexyl) 3-oxobutanoate

1.2 Other means of identification

Product number -
Other names 2-methylcyclohexyl 3-oxobutanoate

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:6624-87-9 SDS

6624-87-9Downstream Products

6624-87-9Relevant academic research and scientific papers

Enantiomer differentiation in intramolecular carbon-hydrogen insertion reactions of racemic secondary alkyl diazoacetates catalyzed by chiral dirhodium(II) carboxamidates

Doyle, M. P.,Kalinin, A. V.

, p. 1729 - 1734 (1995)

Highly efficient kinetic resolution of racemic secondary alkyl diazoacetates in intramolecular carbon-hydrogen insertion reactions has been achieved using chiral dirhodium (II) carboxamidates.Products formed from catalytic diazo decomposition of racemic 2

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