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1,3,2-Diazaborine, 1-ethylhexahydro-2-phenyl- is a complex organic compound with the chemical formula C12H20BN. It is a heterocyclic compound, which means it contains atoms of different elements in its ring structure. Specifically, 1,3,2-Diazaborine, 1-ethylhexahydro-2-phenyl- features a boron atom, two nitrogen atoms, and a phenyl group. The 1-ethylhexahydro part of the name indicates that the compound has a six-carbon chain with a single ethyl group attached, which is fully saturated (hexahydro). 1,3,2-Diazaborine, 1-ethylhexahydro-2-phenyl- is of interest in organic chemistry and materials science due to its unique structure and potential applications in the synthesis of various chemical compounds.

6129-30-2

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6129-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6129-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6129-30:
(6*6)+(5*1)+(4*2)+(3*9)+(2*3)+(1*0)=82
82 % 10 = 2
So 6129-30-2 is a valid CAS Registry Number.

6129-30-2Downstream Products

6129-30-2Relevant 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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