Cas 1258273-66-3,4-(1-fluoro-4-hydroxy-1-nitro-1-(phenylsulfonyl)butan-2-yl)benzonitrile

1258273-66-3

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Basic information

Product Name: 4-(1-fluoro-4-hydroxy-1-nitro-1-(phenylsulfonyl)butan-2-yl)benzonitrile
Synonyms:
CAS NO:1258273-66-3
Molecular Formula:
Molecular Weight: 378.381
EINECS: N/A
Product Categories: N/A
Mol File: 1258273-66-3.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: 4-(1-fluoro-4-hydroxy-1-nitro-1-(phenylsulfonyl)butan-2-yl)benzonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-fluoro-4-hydroxy-1-nitro-1-(phenylsulfonyl)butan-2-yl)benzonitrile(1258273-66-3)
EPA Substance Registry System: 4-(1-fluoro-4-hydroxy-1-nitro-1-(phenylsulfonyl)butan-2-yl)benzonitrile(1258273-66-3)

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: 1258273-66-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1258273-66-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,2,7 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1258273-66:
(9*1)+(8*2)+(7*5)+(6*8)+(5*2)+(4*7)+(3*3)+(2*6)+(1*6)=173
173 % 10 = 3
So 1258273-66-3 is a valid CAS Registry Number.

1258273-66-3Upstream product

95759-33-4 4-cyanocinnamaldehyde

1258273-66-3Downstream Products

1258273-66-3Relevant articles and documents

Highly enantioselective addition of 1-fluoro-1-nitro(phenylsulfonyl)methane to α,β-unsaturated aldehydes

Kamlar, Martin,Bravo, Natalia,Alba, Andrea-Nekane R.,Hybelbauerova, Simona,Cisarova, Ivana,Vesely, Jan,Moyano, Albert,Rios, Ramon

, p. 5464 - 5470 (2010)

An organocatalytic, highly enantioselective addition of 1fluoro-1-nitro(phenylsulfonyl)methane to α,β-unsaturated aldehydes is reported. The reaction is simply catalyzed by secondary amines and furnishes the corresponding fluorinated derivatives in good y

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