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Tris(3-methylbutyl)borane, also known as tris(isopentyl)borane, is an organoborane compound with the chemical formula (C5H11)3B. It is a colorless, viscous liquid that is highly flammable and sensitive to air and moisture. tris(3-methylbutyl)borane is primarily used as a reducing agent in organic synthesis, particularly in the reduction of carbonyl compounds to alcohols. It is also employed as a catalyst in various chemical reactions, such as the hydroboration of alkenes and alkynes. Due to its reactivity, tris(3-methylbutyl)borane is typically handled under an inert atmosphere and stored away from heat and open flames.

3062-81-5

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3062-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3062-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3062-81:
(6*3)+(5*0)+(4*6)+(3*2)+(2*8)+(1*1)=65
65 % 10 = 5
So 3062-81-5 is a valid CAS Registry Number.

3062-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name triisoamylboron

1.2 Other means of identification

Product number -
Other names Triisopentyl-boran

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:3062-81-5 SDS

3062-81-5Relevant academic research and scientific papers

Reaction of organoboranes with hydrazoic acid

Kabalka, George W.,Henderson, David A.,Varma, Rajender S.

, p. 1369 - 1370 (2008/10/08)

Organoboranes react with sodium azide in the presence of aqueous acid to yield primary amines. The reaction presumably proceeds via the anionotropic rearrangement of an organoborate complex.

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