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1,2,3,4,5-pentamethyl-1,2,4,3,5-triazadiborolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31732-41-9

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31732-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31732-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31732-41:
(7*3)+(6*1)+(5*7)+(4*3)+(3*2)+(2*4)+(1*1)=89
89 % 10 = 9
So 31732-41-9 is a valid CAS Registry Number.

31732-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5-pentamethyl-1,2,4,3,5-triazadiborolidine

1.2 Other means of identification

Product number -
Other names pentamethyl-cyclo-1,2,4-triaza-3,5-diborane

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:31732-41-9 SDS

31732-41-9Relevant academic research and scientific papers

Contribution to the Chemistry of Boron, CIX. New Five-Membered Heterocycles of Boron: Triazaborolidines Containing Silicon, Phosphorus and Arsenic as Ring Atoms

Barlos, K.,Noeth, H.

, p. 407 - 414 (2007/10/02)

1,2,4-Triaza-3-sila-5-borolidines (1) are accessible via N,N'-dilithio-N,N'-dimethyl-hydrazine and Br(CH3)B-NCH3-Si(CH3)2Br or by transsilylation of the permethyl derivative of 1.Similarly, phosphorus halides replace the (CH3)2Si group of heptamethyl-triaza-3-sila-5-borolidine (2), affording triaza-3-phospha-5-borolidines, while AsCl3 yields 3-chloro-1,2,4,5-tetramethyl-1,2,4-triaza-3-arsa-5-borolidine.Nucleophilic replacements at the P atom of 3-chloro-triaza-3-phospha-5-borolidine (9) are readily achieved.Surprisingly, the various substituents at the P atom of the new heterocyclic systems have little influence on δ11B, in contrast to δ1H.This is attributed to ?- and ?-effects.It is assumed that the new ring systems are nonplanar. - Keywords: 1,2,4-Triaza-3-sila-5-borolidines, 1,2,4-Triaza-3-phospha-5-borolidines, 1,2,4-Triaza-3-arsa-5-borolidines, NMR Spectra

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