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31029-61-5

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31029-61-5 Usage

General Description

Borin is a chemical compound that consists of a boron atom and three iodine atoms. It is often used as a reagent in organic synthesis reactions and as a source of boron in organic compounds. Borin is a colorless, crystalline solid that is soluble in most organic solvents but insoluble in water. It is known for its mild, selective reactivity and its ability to introduce boron atoms into organic molecules. Borin is commonly used in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its unique reactivity and versatility make it a valuable tool in the advancement of organic chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 31029-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,2 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31029-61:
(7*3)+(6*1)+(5*0)+(4*2)+(3*9)+(2*6)+(1*1)=75
75 % 10 = 5
So 31029-61-5 is a valid CAS Registry Number.

31029-61-5SDS

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 borinine

1.2 Other means of identification

Product number -
Other names BORABENZENE

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:31029-61-5 SDS

31029-61-5Downstream Products

31029-61-5Relevant articles and documents

FROM SILABENZENE TO CYCLOPROPENYLIDENE.

Maier

, p. 95 - 104 (1985)

Isolation and identification of a number of highly reactive species are described. The main route for their preparation involves the combination of flash pyrolysis and matrix isolation in argon at 10 K. This article covers hetero- pi -systems like silabenzene, silaethene, 1,4-disilabenzene, derivatives of borabenzene and boraethene as well as pure carbocyclic compounds with peculiar electronic characteristics. In this context some new aspects of cyclobutadiene-, tetrahedrane- and cyclopentadienone-chemistry are discussed. The main emphasis within this part is directed towards the C//4H//4 potential surface. The article ends with a short comment on cyclopropenylidene.

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