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16924-32-6

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16924-32-6 Usage

General Description

1,1-Dimethyldiborane is a chemical compound with the formula (CH3)2BH. It is a highly reactive and pyrophoric compound, meaning it ignites spontaneously in air. 1,1-Dimethyldiborane is a colorless gas with a strong and unpleasant odor. It is used as a reducing agent in organic synthesis and in the production of boron-containing compounds. Due to its highly reactive nature and the potential for hazardous reactions, it requires careful handling and storage. 1,1-Dimethyldiborane is also used in the development of advanced materials and in the aerospace industry. Overall, it is a valuable compound with specific applications but also poses potential risks due to its reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 16924-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,2 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16924-32:
(7*1)+(6*6)+(5*9)+(4*2)+(3*4)+(2*3)+(1*2)=116
116 % 10 = 6
So 16924-32-6 is a valid CAS Registry Number.

16924-32-6SDS

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 dimethylboranylboron

1.2 Other means of identification

Product number -
Other names 1,1-DIMETHYLDIBORANE

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:16924-32-6 SDS

16924-32-6Relevant articles and documents

Dealkylation of Zirconium(IV) by Borane: The Intimate Mechanism of an Alkyl Transfer Reaction

Marsella, John A.,Caulton, Kenneth G.

, p. 2361 - 2365 (2007/10/02)

The reaction of Cp2ZrMe2 with BH3*THF ultimately yields Cp2Zr(BH4)2.The reaction is sequential in the sense that Cp2Zr(BH4)Me has also been detected.By use of 11B NMR spectroscopy, both for resolution of chemically distinct boron-containing species and as an aid to proton counting, it has been possible to show that these reactions proceed through intermediates containing coordinated BH3Me- and BH2Me2-, and thus the reaction is initially a formal insertion of BH3 into a Zr-CH3 bond.These intermediates react further with borane to produce a complex equilibrating mixture of alkyl diboranes, B2MenH6-n and Zr(BH4) groups.

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