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2-Methyl-2-butyl-1,3-cyclohexanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54644-26-7

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54644-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54644-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,4 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54644-26:
(7*5)+(6*4)+(5*6)+(4*4)+(3*4)+(2*2)+(1*6)=127
127 % 10 = 7
So 54644-26-7 is a valid CAS Registry Number.

54644-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyl-2-methylcyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-n-Butyl-2-methyl-cyclohexan-1,3-dion

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:54644-26-7 SDS

54644-26-7Relevant academic research and scientific papers

A Scalable Protocol for the Regioselective Alkylation of 2-Methylcyclohexane-1,3-dione with Unactivated sp3 Electrophiles

Sharpe, Robert J.,Portillo, Maribel,Vélez, Robert A.,Johnson, Jeffrey S.

supporting information, p. 2293 - 2295 (2015/09/28)

A method for the C-selective alkylation of 2-methylcyclohexane-1,3-dione with unactivated sp3 electrophiles is accomplished via alkylation and subsequent deprotection of the derived ketodimethyl hydrazones. The present method provides a high-yielding entry to dialkyl cycloalkanones that cannot be accessed via direct alkylation of 2-methylcyclohexane-1,3-dione. The title reaction may be useful in the scalable preparation of terpene and steroidal building blocks in the arena of natural product synthesis.

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