Cas 482573-45-5,(2S)-1-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]carbonyl}-1,2-dihydroquinoline-2-carbonitrile

482573-45-5

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Basic information

Product Name: (2S)-1-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]carbonyl}-1,2-dihydroquinoline-2-carbonitrile
Synonyms:
CAS NO:482573-45-5
Molecular Formula:
Molecular Weight: 359.384
EINECS: N/A
Product Categories: N/A
Mol File: 482573-45-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2S)-1-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]carbonyl}-1,2-dihydroquinoline-2-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-1-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]carbonyl}-1,2-dihydroquinoline-2-carbonitrile(482573-45-5)
EPA Substance Registry System: (2S)-1-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]carbonyl}-1,2-dihydroquinoline-2-carbonitrile(482573-45-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 482573-45-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 482573-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,2,5,7 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 482573-45:
(8*4)+(7*8)+(6*2)+(5*5)+(4*7)+(3*3)+(2*4)+(1*5)=175
175 % 10 = 5
So 482573-45-5 is a valid CAS Registry Number.

482573-45-5Upstream product

482573-45-5Downstream Products

482573-45-5Relevant articles and documents

Synthesis of chiral N-protected 1,2-dihydro-quinoline-2-carbonitrile and 1,2-dihydro-isoquinoline-1-carbonitrile via an asymmetric Reissert reaction

Pauvert, Micka?l,Collet, Sylvain C.,Bertrand, Marie-Jo,Guingant, André Y.,Evain, Michel

, p. 2983 - 2987 (2005)

Addition of cyanide ion to chiral N-acyl-quinolinium and N-acyl-isoquinolinium salts led selectively to 1,2-addition products. Removal of the chiral auxiliary affords the title compounds in pure enantiomeric form.

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