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cyclohex-3-enyl(trimethylsilyloxy)acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85906-00-9

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85906-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85906-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,0 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85906-00:
(7*8)+(6*5)+(5*9)+(4*0)+(3*6)+(2*0)+(1*0)=149
149 % 10 = 9
So 85906-00-9 is a valid CAS Registry Number.

85906-00-9Relevant academic research and scientific papers

Niobium fluoride (NbF5): A highly efficient catalyst for solvent-free cyanosilylation of aldehydes

Sung, Soo Kim,Rajagopal, Gurusamy

, p. 215 - 218 (2007/10/03)

An efficient method for the addition of trimethylsilylcyanide (TMSCN) to aldehydes using dispersed NbF5 as the catalyst is described. Cyano transfer from TMSCN to aldehydes occurs within 10 minutes at room temperature in the presence of 0.5 mol

N-methylmorpholine N-oxide: A rare nonmetallic catalyst for the most efficient silylcyanation of aldehydes

Kim, Sung Soo,Rajagopal, Gurusamy,Kim, Dong Won,Song, Dae Ho

, p. 2973 - 2980 (2007/10/03)

An efficient method of addition of trimethylsilyl cyanide (TMSCN) to aldehydes by employing N-methylmorpholine N-oxide (NMO) alone as the catalyst has been described. Most of aromatic, aliphatic, cyclic, and heterocyclic aldehydes have been converted into

Enzymatic Preparation of Optically Active Cyanohydrin Acetates

Almsick, Andreas van,Buddrus, Joachim,Hoenicke-Schmidt, Petra,Laumen, Kurt,Schneider, Manfred P.

, p. 1391 - 1393 (2007/10/02)

A series of cyanohydrin acetates (1)-(47) of widely varying structures, potential chiral building blocks for numerous synthetic applications, has been prepared in good chemical and often high optical yields by enzymatic hydrolysis of their racemic acetates in the presence of an ester hydrolase from Pseudomonas sp.

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