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1,3-dimethyl-2-phenyl-1,3,2-diazaboracycloheptane is a complex organic compound with the molecular formula C13H18BN3. It is a derivative of diazaboracycloheptane, which is a type of boron-containing heterocycle. This specific compound features a seven-membered ring structure with a boron atom at one end, two nitrogen atoms, and a phenyl group attached to one of the carbon atoms. The two methyl groups are attached to the adjacent carbon atoms, making the structure more sterically hindered. 1,3-dimethyl-2-phenyl-1,3,2-diazaboracycloheptane is of interest in the field of organoboron chemistry, as it can be used as a ligand in various catalytic reactions and as a building block for more complex molecules. Its unique structure and properties make it a valuable tool for researchers in the synthesis of pharmaceuticals, materials, and other specialty chemicals.

6063-77-0

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6063-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6063-77-0 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 6063-77:
(6*6)+(5*0)+(4*6)+(3*3)+(2*7)+(1*7)=90
90 % 10 = 0
So 6063-77-0 is a valid CAS Registry Number.

6063-77-0Downstream Products

6063-77-0Relevant 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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