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3-Hexene, 2,3-dimethyl-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59643-75-3

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59643-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59643-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,4 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59643-75:
(7*5)+(6*9)+(5*6)+(4*4)+(3*3)+(2*7)+(1*5)=163
163 % 10 = 3
So 59643-75-3 is a valid CAS Registry Number.

59643-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethylhex-3-ene

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-3-hexene

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:59643-75-3 SDS

59643-75-3Downstream Products

59643-75-3Relevant academic research and scientific papers

Scope and Regiochemical Control of the Allylpotassium Reaction in the Synthesis of Sterols with Unsaturated Side Chains

Giner, Jose-Luis,Margot, Christian,Djerassi, Carl

, p. 2117 - 2125 (2007/10/02)

Allylpotassium derivatives were prepared from a variety of olefins by using Schlosser's base (BuLi/KOt-Bu).Reaction with (20S)-20-(iodomethyl)pregnane i-methyl ether (1) followed by deprotection gave in high yields a wide variety of Δ24 and Δ24(28) sterols, including the naturally occuring desmosterol (37), fucosterol (33), 24(E)-propylidenecholesterol (35), 24-methylenecholesterol (3), dehydroaplysterol (10), 25-methyl-24-methylenecholesterol (11), mutasterol (12), and 25-methylxestosterol (13).Control of the regiochemistry of unsymmetrical allylmetals was achieved through the addition of Li2CuCl3.Rules concerning the high regioselectivities and stereoselectivities are discussed.

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