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1,2,3-trimethyl-[1,3,2]diazaborinane is a chemical compound with the molecular formula C3H9BN2. It is a heterocyclic compound consisting of a boron atom, two nitrogen atoms, and three methyl groups. 1,2,3-trimethyl-[1,3,2]diazaborinane is known for its reactivity and is often used as a reducing agent in organic synthesis. It is particularly effective in the reduction of carbonyl compounds to form alcohols, a process known as the Meerwein-Ponndorf-Verley reduction. The compound's structure and reactivity make it a valuable tool in the synthesis of various organic compounds, and it is also used in the preparation of other boron-containing reagents.

5898-36-2

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5898-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5898-36-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5898-36:
(6*5)+(5*8)+(4*9)+(3*8)+(2*3)+(1*6)=142
142 % 10 = 2
So 5898-36-2 is a valid CAS Registry Number.

5898-36-2Downstream Products

5898-36-2Relevant 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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