Cas 278605-46-2,(2S,4S,5R)-2-[(1S)-Fluoro(2-naphthyl)methyl]-3,4-dimethyl-2-oxo-5-phenyl-1,3,2λ<sup>5</sup>-oxazaphospholidine

278605-46-2

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Basic information

Product Name: (2S,4S,5R)-2-[(1S)-Fluoro(2-naphthyl)methyl]-3,4-dimethyl-2-oxo-5-phenyl-1,3,2λ⁵-oxazaphospholidine
Synonyms:
CAS NO:278605-46-2
Molecular Formula:
Molecular Weight: 369.375
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: (2S,4S,5R)-2-[(1S)-Fluoro(2-naphthyl)methyl]-3,4-dimethyl-2-oxo-5-phenyl-1,3,2λ⁵-oxazaphospholidine(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S,5R)-2-[(1S)-Fluoro(2-naphthyl)methyl]-3,4-dimethyl-2-oxo-5-phenyl-1,3,2λ⁵-oxazaphospholidine(278605-46-2)
EPA Substance Registry System: (2S,4S,5R)-2-[(1S)-Fluoro(2-naphthyl)methyl]-3,4-dimethyl-2-oxo-5-phenyl-1,3,2λ⁵-oxazaphospholidine(278605-46-2)

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: 278605-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 278605-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,8,6,0 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 278605-46:
(8*2)+(7*7)+(6*8)+(5*6)+(4*0)+(3*5)+(2*4)+(1*6)=172
172 % 10 = 2
So 278605-46-2 is a valid CAS Registry Number.

278605-46-2Upstream product

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278605-46-2Relevant academic research and scientific papers

Preparation of chiral α-monofluoroalkylphosphonic acids and their evaluation as inhibitors of protein tyrosine phosphatase 1B

Kotoris, Christopher C.,Wen, Wcndy,Lough, Alan,Taylor, Scott D.

, p. 1271 - 1281 (2007/10/03)

Enantiomerically pure α-monofluoroalkylphosphonic acids 4-9 were synthesized by diastereoselective electrophilic fluorination of α-carbanions of asymmetric phosphonamidates bearing (-)-ephedrine as a chiral auxiliary. The diastereomeric excess of the fluo

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