Cas 211444-56-3,(S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one

211444-56-3

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Basic information

Product Name: (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one
Synonyms: (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one
CAS NO:211444-56-3
Molecular Formula:
Molecular Weight: 315.344
EINECS: N/A
Product Categories: N/A

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: (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one(211444-56-3)
EPA Substance Registry System: (S)-4-Benzyl-3-((1S,2S,4S)-2-fluoro-bicyclo[2.2.1]hept-5-ene-2-carbonyl)-oxazolidin-2-one(211444-56-3)

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: 211444-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 211444-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,4,4 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 211444-56:
(8*2)+(7*1)+(6*1)+(5*4)+(4*4)+(3*4)+(2*5)+(1*6)=93
93 % 10 = 3
So 211444-56-3 is a valid CAS Registry Number.

211444-56-3Upstream product

90719-32-7 (S)-4-Benzyl-2-oxazolidinone

211444-56-3Downstream Products

211444-56-3Relevant academic research and scientific papers

Asymmetric Diels-Alder reactions of 2-fluoroacrylic acid derivatives. Part 1: The construction of fluorine substituted chiral tertiary carbon

Ito, Hisanaka,Saito, Akio,Taguchi, Takeo

, p. 1979 - 1987 (2007/10/03)

For the construction of chiral monofluorinated tertiary carbons, we have examined the asymmetric Diels-Alder reaction of 2-fluoroacrylic acid derivatives beating a chiral oxazolidinone moiety. Under diethylaluminum chloride catalyzed conditions at - 100°C

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