Cas 158221-61-5,(4R)-4-Phenyl-4,6,7,8-tetrahydro-3H-pyrido<2,1-c><1,4>oxazin-1-one

158221-61-5

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Basic information

Product Name: (4R)-4-Phenyl-4,6,7,8-tetrahydro-3H-pyrido<2,1-c><1,4>oxazin-1-one
Synonyms: (4R)-4-Phenyl-4,6,7,8-tetrahydro-3H-pyrido<2,1-c><1,4>oxazin-1-one
CAS NO:158221-61-5
Molecular Formula:
Molecular Weight: 229.279
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: (4R)-4-Phenyl-4,6,7,8-tetrahydro-3H-pyrido<2,1-c><1,4>oxazin-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R)-4-Phenyl-4,6,7,8-tetrahydro-3H-pyrido<2,1-c><1,4>oxazin-1-one(158221-61-5)
EPA Substance Registry System: (4R)-4-Phenyl-4,6,7,8-tetrahydro-3H-pyrido<2,1-c><1,4>oxazin-1-one(158221-61-5)

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: 158221-61-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 158221-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,2,2 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 158221-61:
(8*1)+(7*5)+(6*8)+(5*2)+(4*2)+(3*1)+(2*6)+(1*1)=125
125 % 10 = 5
So 158221-61-5 is a valid CAS Registry Number.

158221-61-5Upstream product

500131-75-9 (4R)-4-Phenylhexahydropyrido<2,1-c><1,4>oxazin-1-one

158221-61-5Downstream Products

158221-61-5Relevant academic research and scientific papers

Asymmetric Synthesis. 32. A New Access to Enantiomerically Pure (S)-(-)-Pipecolic Acid and 2- or 6-Alkylated Derivatives

Berrien, J. -F.,Royer, J.,Husson, H. -P.

, p. 3769 - 3774 (1994)

Enantiomerically pure (S)-(-)-pipecolic acid (5) was synthesized in four steps and 47percent overall yield starting from 2-cyano-6-phenyloxazolopiperidine (1).A general strategy is described for preparing 2-alkylated and 6-alkylated pipecolic acid 7a-c and 11a-c using diastereoselective procedures.

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