Cas 173167-66-3,(4R,6aR,9aS,9bS)-4,8,9b-Triphenyl-hexahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-c][1,4]oxazine-1,7,9-trione

173167-66-3

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Basic information

Product Name: (4R,6aR,9aS,9bS)-4,8,9b-Triphenyl-hexahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-c][1,4]oxazine-1,7,9-trione
Synonyms: (4R,6aR,9aS,9bS)-4,8,9b-Triphenyl-hexahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-c][1,4]oxazine-1,7,9-trione
CAS NO:173167-66-3
Molecular Formula:
Molecular Weight: 438.483
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,6aR,9aS,9bS)-4,8,9b-Triphenyl-hexahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-c][1,4]oxazine-1,7,9-trione(CAS DataBase Reference)
NIST Chemistry Reference: (4R,6aR,9aS,9bS)-4,8,9b-Triphenyl-hexahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-c][1,4]oxazine-1,7,9-trione(173167-66-3)
EPA Substance Registry System: (4R,6aR,9aS,9bS)-4,8,9b-Triphenyl-hexahydro-pyrrolo[3',4':3,4]pyrrolo[2,1-c][1,4]oxazine-1,7,9-trione(173167-66-3)

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: 173167-66-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 173167-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,1,6 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 173167-66:
(8*1)+(7*7)+(6*3)+(5*1)+(4*6)+(3*7)+(2*6)+(1*6)=143
143 % 10 = 3
So 173167-66-3 is a valid CAS Registry Number.

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173167-66-3Relevant academic research and scientific papers

Synthesis of α-Phenyl Proline Derivatives via 1,3-Dipolar Cycloaddition of Chiral Stabilised Azomethine Ylids.

Anslow, Amberley. S.,Harwood, Laurence. M.,Lilley, Ian. A.

, p. 2465 - 2468 (2007/10/03)

The preparation of (3S,5R)-3,5-diphenylmorpholinone 1 and subsequent diastereoselective 1,3-dipolar cycloaddition of its formaldehyde derived azomethine ylid is described.Removal of the chiral template furnishes α-phenyl proline derivatives.

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