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2-Decanol, 1,1-dichloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52183-67-2

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52183-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52183-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52183-67:
(7*5)+(6*2)+(5*1)+(4*8)+(3*3)+(2*6)+(1*7)=112
112 % 10 = 2
So 52183-67-2 is a valid CAS Registry Number.

52183-67-2SDS

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 1,1-dichloro-2-decanol

1.2 Other means of identification

Product number -
Other names 1,1-dichloro-decan-2-ol

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:52183-67-2 SDS

52183-67-2Upstream product

52183-67-2Relevant academic research and scientific papers

Process for the preparation of cyclopropylacetylene

-

, (2008/06/13)

The present invention relates generally to novel methods for the synthesis of cyclopropylacetylene which is an essential reagent in the asymmetric synthesis of (S)-6-chloro-4-cyclopropylethynyl-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one; a useful human immunodeficiency virus (HIV) reverse transcriptase inhibitor. In the process, for example, cyclopropane carboxaldehyde is alkylated to form 1,1,1-trichloro-2-cyclopropyl-ethanol; which in turn is hydroxy protected to form 1,1,1-trichloro-2-cyclopropylethyltosylate; which in turn undergoes elimination to form cyclopropyl acetylene. This improvement provides for high conversion of inexpensive, readily available starting materials into cyclopropylacetylene, high overall yields and can be conducted on an industrial scale.

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