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1-Cyclopentyl-borinane, also known as 1-cyclopentyl-3,4-dimethyl-2,5-dihydro-1H-borine, is an organoborane compound with the chemical formula C9H17B. It is a colorless liquid that is soluble in organic solvents and is widely used as a reducing agent in organic synthesis, particularly in the reduction of carbonyl compounds to alcohols. The compound is known for its high reactivity and selectivity, making it a valuable tool in the synthesis of various pharmaceuticals and natural products. It is also used in the preparation of other organoborane reagents and as a ligand in transition metal catalysis. Due to its sensitivity to air and moisture, 1-cyclopentyl-borinane is typically handled under an inert atmosphere.

5747-19-3

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5747-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5747-19-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5747-19:
(6*5)+(5*7)+(4*4)+(3*7)+(2*1)+(1*9)=113
113 % 10 = 3
So 5747-19-3 is a valid CAS Registry Number.

5747-19-3Downstream Products

5747-19-3Relevant academic research and scientific papers

Hydroboration Kinetics. 10. Kinetics, Mechanism, and Selectivity for Hydroboration of Representative Alkenes with Borinane

Brown, Herbert C.,Chandrasekharan, J.,Nelson, Donna J.

, p. 3768 - 3771 (1984)

The kinetics of hydroboration of representative alkenes with borinane dimer have been studied at 0 deg C in n-heptane.With many alkenes the reaction shows three-halves-order rate behavior, indicating a fast dissociation of the borinane dimer, followed by the rate-limiting step involving the monomer and the alkene.With a few alkenes the reaction was too fast for accurate rate measurements.The rate data indicate a possible generalization of the earlier conclusions for the mechanism of hydroboration of alkenes by 9-borabicyclononane dimer, (9-BBN)2.The relative rates calculated from the rate constants agree well with those determined competitively.A comparison of the reactivity of borinane toward various classes of alkenes with those of other hydroborating agents, such as 9-BBN, disiamylborane, dibromoborane-methyl sulfide, and thexylchloroborane-methyl sulfide, shows that borinane is similar to 9-BBN in its selectivity and differs markedly from that of disiamylborane, dibromoborane-methyl sulfide, and thexylchloroborane-methyl sulfide.

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