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24251-76-1

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24251-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24251-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24251-76:
(7*2)+(6*4)+(5*2)+(4*5)+(3*1)+(2*7)+(1*6)=91
91 % 10 = 1
So 24251-76-1 is a valid CAS Registry Number.

24251-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-cyclohexylpentan-1-one

1.2 Other means of identification

Product number -
Other names 2-chloro-1-cyclohexyl-1-pentanone

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:24251-76-1 SDS

24251-76-1Downstream Products

24251-76-1Relevant articles and documents

1-Haloalkyl Aryl Sulfoxides as Useful Agents in Synthesis of α-Halo Ketones: A New Synthesis of α-Halo Ketones, α-Halo α,β-Unsaturated Ketones, and α-Halo Cross Dienones from Aldehydes

Satoh, Tsuyoshi,Itoh, Norifumi,Onda, Ken-ichi,Kitoh, Yasushi,Yamakawa, Koji

, p. 2800 - 2806 (2007/10/02)

α-Halo α-sulfinyl ketones were synthesized in two steps from 1-haloalkyl aryl sulfoxides and aldehydes in high yields.Desulfinylation of the α-halo α-sulfinyl ketones was performed with ethylmagnesium bromide in ether at low temperature to afford α-halo ketones via magnesium enolates in high yields.The magnesium enolate intermediates were trapped with various electrophiles such as deuterium oxide, ethyl chloroformate, and chlorotrimethylsilane.Trapping of the magnesium enolate intermediate with carbonyl compounds afforded a new type of the directed aldol reaction.Desulfi nylation of the sulfinyl group of the α-halo α-sulfinyl ketones under thermal conditions gave α-halo α,β-unsatureted ketones or α-halo cross dienones.

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