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Cyclohexane, (1-bromo-1-hexenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67532-05-2

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67532-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67532-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,3 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67532-05:
(7*6)+(6*7)+(5*5)+(4*3)+(3*2)+(2*0)+(1*5)=132
132 % 10 = 2
So 67532-05-2 is a valid CAS Registry Number.

67532-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-bromo-1-cyclohexyl-1-hexene

1.2 Other means of identification

Product number -
Other names ((Z)-1-Bromo-hex-1-enyl)-cyclohexane

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:67532-05-2 SDS

67532-05-2Downstream Products

67532-05-2Relevant academic research and scientific papers

The Reactions of (1-Halo-1-alkenyl)dialkylboranes with Lead(IV) Acetate or (Diacetoxyiodo)benzene. A Stereoselective Synthesis of 1-Halo-1,2-dialkylethylenes

Masuda, Yuzuru,Arase, Akira,Suzuki, Akira

, p. 1652 - 1655 (2007/10/02)

The reaction of (1-halo-1-alkenyl)dialkylboranes with lead(IV) acetate or (diacetoxyiodo)benzene was studied. (1-Bromo-1-alkenyl)dialkylboranes gave 1-bromo-1,2-dialkylethylenes.When alkyl groups on the boron atom of vinylboranes were bulky or the reaction temperatures were low, Z-isomers were afforded, whereas when alkyl groups on the boron atom were small or the reaction temperatures were relatively high, E-isomers were afforded as the main products. (1-Chloro-1-alkenyl)dialkylboranes gave (Z)-1-chloro-1,2-dialkylethylenes regardless of the reaction conditions. (1-Iodo-1-alkenyl)dialkylboranes failed to give satisfactory yields of 1-iodo-1,2-dialkylethylenes.

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