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Borane, dicyclohexyl(1-methyl-1-hexenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92747-34-7

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92747-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92747-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,4 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92747-34:
(7*9)+(6*2)+(5*7)+(4*4)+(3*7)+(2*3)+(1*4)=157
157 % 10 = 7
So 92747-34-7 is a valid CAS Registry Number.

92747-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Dicyclohexyl-((E)-1-methyl-hex-1-enyl)-borane

1.2 Other means of identification

Product number -
Other names -

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:92747-34-7 SDS

92747-34-7Downstream Products

92747-34-7Relevant academic research and scientific papers

THE SYNTHESIS OF REGIO- AND STEREOSPECIFICALLY SUBSTITUTED 1,4-DIENES OR CONJUGATED ENYENES FROM INTERNAL ALKENYLDIALKYLBORANES

Hoshi, Masayuki,Masuda, Yuzuru,Nunokawa, Yutaka,Arase, Akira

, p. 1029 - 1032 (2007/10/02)

Internal alkenyldialkylboranes give regio- and stereospecifically desidgned 1,4-dienes or conjugated enyenes, bearing a substituent at the internal alkenyl carbon atom, by a coupling reaction with allyl bromide or 1-bromo-1-alkynes.

NOVEL SYNTHESIS OF INTERNAL ALKENYLDIALKYLBORANE BY THE REACTION OF 1-HALO-1-ALKENYLDIALKYLBORANE WITH GRIGNARD REAGENT.

Arase,Hoshi,Masuda

, p. 209 - 213 (2007/10/02)

To synthesize internal alkenyldialkylboranes, coupling reactions were carried out by using 1-halo-1-alkenyldialkylboranes and Grignard reagents. Hydrogen peroxide oxidation and protonolysis with acetic acid of the reaction product revealed that internal (E)-alkenyldialkylborane was formed in 60-90% yield.

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