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1,2,3-trimethyl-1,3,2-diazaboracycloheptane is a complex organic compound with the molecular formula C6H15BN2. It is a derivative of diazaboracycloheptane, featuring three methyl groups attached to the carbon atoms at positions 1, 2, and 3. 1,2,3-trimethyl-1,3,2-diazaboracycloheptane is known for its unique structure, which includes a boron atom bonded to two nitrogen atoms, forming a seven-membered ring. It is of interest in the field of organoboron chemistry due to its potential applications in the synthesis of various organic compounds and as a ligand in catalysis. The compound's stability and reactivity can be influenced by the presence of the methyl groups, making it a subject of study for understanding the effects of substituents on the properties of diazaboracycloheptane derivatives.

6063-70-3

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6063-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6063-70-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6063-70:
(6*6)+(5*0)+(4*6)+(3*3)+(2*7)+(1*0)=83
83 % 10 = 3
So 6063-70-3 is a valid CAS Registry Number.

6063-70-3Downstream Products

6063-70-3Relevant 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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