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1-[chloro(phenylsulfinyl)methyl]cyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21849-27-4

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21849-27-4 Usage

Functional groups

Cyclohexanol, phenylsulfinyl, chloro

Structure

A cyclohexanol derivative with a phenylsulfinyl and a chloro group attached to the carbon atom

Usage

Organic synthesis

Role

Chiral auxiliary in asymmetric synthesis

Applications

Pharmaceutical industry for the synthesis of chiral drugs and other bioactive compounds

Value

Research and development of new chemical processes and products

Check Digit Verification of cas no

The CAS Registry Mumber 21849-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,4 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21849-27:
(7*2)+(6*1)+(5*8)+(4*4)+(3*9)+(2*2)+(1*7)=114
114 % 10 = 4
So 21849-27-4 is a valid CAS Registry Number.

21849-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[benzenesulfinyl(chloro)methyl]cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(Phenylsulfinylchlormethyl)-cyclohexanol

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:21849-27-4 SDS

21849-27-4Relevant academic research and scientific papers

α-Sulfinyl carbenoid: One-carbon homologation of ketones to α-sulfinyl ketones using chloromethyl phenyl sulfoxide

Satoh, Tsuyoshi,Hayashi, Yasumasa,Mizu, Yasuhiro,Yamakawa, Koji

, p. 7181 - 7184 (2007/10/02)

Addition of the carbanion of chloromethyl phenyl sulfoxide to ketones gave the adducts, which were treated with lithium diisopropylamide to afford one-carbon homologated α-sulfinyl ketones via α-sulfinyl carbenoids in moderate to high yields.

α,β-Epoxy Sulfoxides as Useful Intermediates in Organic Synthesis. I. A Novel Synthesis of Dialkyl Ketones and a Synthesis of Aldehydes from Ketones by One Carbon Elongation

Satoh, Tsuyoshi,Kaneko, Youhei,Izawa, Takao,Sakata, Kiichi,Yamakawa, Koji

, p. 1983 - 1990 (2007/10/02)

Treatment of α,β-epoxy sulfoxides, prepared from 1-chloroalkyl phenyl sulfoxides with ketones or aldehydes, with sodium benzeneselenolate gives dialkyl ketones or aldehydes in good yields under mild conditions.The mechanism of this reaction and an application of this process to a formal total synthesis of dihydrojasmone are described.

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