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9-Borabicyclo[3.3.1]nonane, 9-[2-methyl-4-(phenylmethoxy)butyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141361-97-9

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141361-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141361-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,6 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141361-97:
(8*1)+(7*4)+(6*1)+(5*3)+(4*6)+(3*1)+(2*9)+(1*7)=109
109 % 10 = 9
So 141361-97-9 is a valid CAS Registry Number.

141361-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(2-methyl-4-phenylmethoxybutyl)-9-borabicyclo[3.3.1]nonane

1.2 Other means of identification

Product number -
Other names 9-Borabicyclo[3.3.1]nonane,9-[2-methyl-4-(phenylmethoxy)butyl]

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:141361-97-9 SDS

141361-97-9Relevant academic research and scientific papers

Copper-catalyzed carboxylation of alkylboranes with carbon dioxide: Formal reductive carboxylation of terminal alkenes

Ohmiya, Hirohisa,Tanabe, Masahito,Sawamura, Masaya

supporting information; experimental part, p. 1086 - 1088 (2011/04/23)

Carboxylation of alkylboron compounds (alkyl-9-BBN) with CO2 proceeded in the presence of catalytic amounts of CuOAc/1,10-phenanthroline and a stoichiometric amount of KOtBu. The alkylboranes are easily and widely available through the alkene hydroboration, and thus the overall process represents a reductive carboxylation of alkenes with CO2. The broad functional group compatibility and the inexpensiveness of the Cu/1,10-phenathoroline catalyst system are attractive features of this protocol.(Figure Presented)

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