Cas 176965-57-4,(3aS,4aR,7S,8aS,8bR)-7-Phenyl-3-(3-phenyl-propionyl)-hexahydro-[1,3]dioxino[4',5':4,5]furo[2,3-d]oxazol-2-one

176965-57-4

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Basic information

Product Name: (3aS,4aR,7S,8aS,8bR)-7-Phenyl-3-(3-phenyl-propionyl)-hexahydro-[1,3]dioxino[4',5':4,5]furo[2,3-d]oxazol-2-one
Synonyms:
CAS NO:176965-57-4
Molecular Formula:
Molecular Weight: 395.412
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: (3aS,4aR,7S,8aS,8bR)-7-Phenyl-3-(3-phenyl-propionyl)-hexahydro-[1,3]dioxino[4',5':4,5]furo[2,3-d]oxazol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4aR,7S,8aS,8bR)-7-Phenyl-3-(3-phenyl-propionyl)-hexahydro-[1,3]dioxino[4',5':4,5]furo[2,3-d]oxazol-2-one(176965-57-4)
EPA Substance Registry System: (3aS,4aR,7S,8aS,8bR)-7-Phenyl-3-(3-phenyl-propionyl)-hexahydro-[1,3]dioxino[4',5':4,5]furo[2,3-d]oxazol-2-one(176965-57-4)

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: 176965-57-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176965-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,9,6 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 176965-57:
(8*1)+(7*7)+(6*6)+(5*9)+(4*6)+(3*5)+(2*5)+(1*7)=194
194 % 10 = 4
So 176965-57-4 is a valid CAS Registry Number.

176965-57-4Upstream product

176965-57-4Downstream Products

176965-57-4Relevant academic research and scientific papers

D-xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective alkylations

Koell, Peter,Luetzen, Arne

, p. 637 - 640 (1996)

Chiral N-acylated oxazolidin-2-ones readily available from D-xylose have been demonstrated to undergo highly diastereoselective alkylation reactions via their lithium imide enolates to afford α-branched products. These are easily purified and hydrolyzed w

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