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(1S,2R,5S,6R)-3-azatricyclo[4.2.1.02,5]nonan-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

179462-35-2

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179462-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179462-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,4,6 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 179462-35:
(8*1)+(7*7)+(6*9)+(5*4)+(4*6)+(3*2)+(2*3)+(1*5)=172
172 % 10 = 2
So 179462-35-2 is a valid CAS Registry Number.

179462-35-2Downstream Products

179462-35-2Relevant academic research and scientific papers

Vapour-assisted enzymatic hydrolysis of β-lactams in a solvent-free system

Forro, Eniko,Fueloep, Ferenc

, p. 1005 - 1009 (2008/09/21)

A new, solvent-free, vapour-assisted method, developed for the synthesis of carbocyclic cis β-amino acid enantiomers through the Candida antarctica lipase B-catalysed enantioselective (E >200) hydrolysis of β-lactams with 0.5 equiv of H2O at 70 °C, has been demonstrated to be applicable on a preparative scale to produce (±)-2 (the starting racemate for cispentacin), (±)-3 (the starting racemate for 4-tert-butylcispentacin, a new cispentacin analogue) and (±)-7 (the starting racemate for 1,4-ethylene-bridged cispentacin).

Synthesis of enantiopure 1,4-ethyl- and 1,4-ethylene-bridged cispentacin by lipase-catalyzed enantioselective ring opening of β-lactams

Forro, Eniko,Fueloep, Ferenc

, p. 573 - 575 (2007/10/03)

1,4-Ethyl- and 1,4-ethylene-bridged cispentacin enantiomers 1a, 1c and 2a, 2c were prepared through the lipase-catalyzed enantioselective ring opening of racemic exo-3-azatricyclo[4.2.1.02.5]nonan-4-one, (±)-1, and exo-3-azatricyclo[4.2.1.02.5]non-7-en-4-one, (±)-2. High enantioselectivity (E >200) was observed when the Lipolase-catalyzed reactions were performed with 1equiv of H2O in diisopropyl ether at 70°C. The resolved β-amino acids 1a and 2a (yield 46%) and β-lactams 1b and 2b (yield≥40%) could be easily separated. The ring opening of lactam enantiomers with 18% HCl afforded the corresponding β-amino acid hydrochloride enantiomers (ee ≥98%).

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