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Cyclohexanone, 2-acetyl-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14580-53-1

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14580-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14580-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,8 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14580-53:
(7*1)+(6*4)+(5*5)+(4*8)+(3*0)+(2*5)+(1*3)=101
101 % 10 = 1
So 14580-53-1 is a valid CAS Registry Number.

14580-53-1SDS

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 2-acetyl-3-methylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-acetyl-3-methylcyclohexanone

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:14580-53-1 SDS

14580-53-1Downstream Products

14580-53-1Relevant academic research and scientific papers

Platinum(II)/europium(III)-catalyzed intramolecular hydroalkylation of 4-pentenyl β-dicarbonyl compounds

Liu, Cong,Widenhoefer, Ross A.

, p. 285 - 287 (2007/10/03)

A mixture of [PtCl2(CH2CH2)]2 (1 mol %), and EuCl3 (2 mol %) catalyzes the hydroalkylation of 4-pentenyl β-dicarbonyl compounds to form substituted cyclohexanones in moderate to excellent yield with e

TRAPPING REACTION OF ENOLATES FROM LITHIUM DIMETHYLCUPRATE CONJUGATED ADDITION: IMPORTANCE OF STERIC FACTORS AND, PARTICULARLY, OF β-SUBSTITUTION OF ENONE IN THE C- vs. O-ACYLATION

Bernasconi, Silvana,Jommi, Giancarlo,Montanari, Stefania,Sisti, Massimo

, p. 125 - 128 (2007/10/02)

Conjugated addition of lithium dimethylcuprate to α,β-unsaturated ketones gives intermediate enolates which, treated with acetyl chloride, undergo O- and/or C-acylation depending on the substitution at the enone β-carbon.Results agree with the hypothesis that C-acylation proceeds through an intramolecular metal-assisted mechanism.

C-acylation of enolates from lithium dimethylcuprate addition to α,β-unsaturated ketones

Bernasconi,Gariboldi,Jommi,Sisti

, p. 2337 - 2340 (2007/10/02)

The enolates from 1,4 addition of lithium dimethylcuprate to 2-cyclohexenone, 2-cyclopentenone and methyl vinyl ketone, with acetyl chloride, give only C-acylated products and not O-acylated products as previously reported in literature.

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