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107134-81-6

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107134-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107134-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,3 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107134-81:
(8*1)+(7*0)+(6*7)+(5*1)+(4*3)+(3*4)+(2*8)+(1*1)=96
96 % 10 = 6
So 107134-81-6 is a valid CAS Registry Number.

107134-81-6SDS

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 dichloro-(2-dichloroboranylphenyl)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:107134-81-6 SDS

107134-81-6Relevant articles and documents

Unlocking metal coordination of diborylamides through ring constraints

Brown, W. Kice,Klausmeyer, Kevin K.,Lindley, Brian M.

, p. 867 - 870 (2022/02/01)

A cyclic lithium diborylamide compound was synthesized and crystallographically characterized, revealing strong Li–N bonding in sharp contrast to previous linear diborylamides. Two iron(ii) diborylamide complexes were also synthesized, including a 2-coordinate Fe bis(diborylamide) complex. The present cyclic diborylamide represents a new addition to the growing scope of amide ligands.

Borylation of Arylsilanes, II. - Synthesis and Reactions of Silylated Dihalogenphenylboranes

Kaufmann, Dieter

, p. 901 - 906 (2007/10/02)

Upon treatment with trihaloboranes 4a and 4b the bissilylated benzenes 1, 2, and 3 yield the silylated dihalogenphenylboranes 5a-7b under substitution of one silyl group only.The corresponding difluoroboranes 5c-7c are easily accessible by a new fluorination method under mild reaction conditions by treating the dichloroboranes with lithium fluoride in ether.Upon heating with excess 4 the exchange of the second silyl group occurs, too, yielding the position-isomeric diborylbenzenes 9, 10, and 11.The bromination of the silylated dichlorophenylboranes 5a-7a proceeds with high regioselectivity under desilylation yielding 12, 13, and 14.The dimethoxyboranes 15, 16, and 17, synthesized by methanolysis of the corresponding dichloroboranes, can be coupled with bromobenzene under palladium(0) catalysis to yield the position-isomeric silylated biphenyls 18, 19, and 20.

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