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2-butyl-1,3-diethyl-[1,3,2]diazaborolidine is a complex organic compound with the molecular formula C9H22BN3. It is a derivative of [1,3,2]diazaborolidine, which is a type of boron-containing heterocycle. This specific compound features a butyl group at the 2-position, and two ethyl groups at the 1 and 3 positions. It is known for its potential applications in organic synthesis, particularly as a chiral auxiliary or ligand in asymmetric catalysis, where it can help to control the stereochemistry of reactions. The compound's structure and properties make it a valuable tool in the development of enantioselective synthetic methods.

6167-19-7

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6167-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6167-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6167-19:
(6*6)+(5*1)+(4*6)+(3*7)+(2*1)+(1*9)=97
97 % 10 = 7
So 6167-19-7 is a valid CAS Registry Number.

6167-19-7SDS

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 2-butyl-1,3-diethyl-[1,3,2]diazaborolidine

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

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More Details:6167-19-7 SDS

6167-19-7Downstream Products

6167-19-7Relevant academic research and scientific papers

Boron-nitrogen compounds. XXV. Substituted 1,3,2-diazaboracycloalkanes

Weber, Wolfgang,Dawson, John W.,Niedenzu, Kurt

, p. 726 - 728 (2008/10/08)

Boron- and nitrogen-substituted 1,3,2-diazaboracycloalkanes have been prepared by a transamination between bis(dimethylamino)boranes and α,ω-diamines. Partial substitution of the nitrogen of the diamine does not appear to inhibit this reaction; five-, six-, and seven-membered heterocyclic systems are readily obtained by the described procedure. However, the low yields of product obtained in those reactions involving an olefinic α,ω-diamine indicate that steric factors may play an important role. The mechanism of the formation of the boron-nitrogen-carbon heterocycles is discussed, and some spectroscopic data are briefly evaluated.

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