Cas 285568-38-9,2,2-Dimethyl-propionic acid (3aS,5R,6S,6aR)-5-[(R)-1,2-bis-(2,2-dimethyl-propionyloxy)-ethyl]-2-oxo-3-phenylacetyl-hexahydro-furo[2,3-d]oxazol-6-yl ester

285568-38-9

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Basic information

Product Name: 2,2-Dimethyl-propionic acid (3aS,5R,6S,6aR)-5-[(R)-1,2-bis-(2,2-dimethyl-propionyloxy)-ethyl]-2-oxo-3-phenylacetyl-hexahydro-furo[2,3-d]oxazol-6-yl ester
Synonyms: 2,2-Dimethyl-propionic acid (3aS,5R,6S,6aR)-5-[(R)-1,2-bis-(2,2-dimethyl-propionyloxy)-ethyl]-2-oxo-3-phenylacetyl-hexahydro-furo[2,3-d]oxazol-6-yl ester
CAS NO:285568-38-9
Molecular Formula:
Molecular Weight: 575.656
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: 2,2-Dimethyl-propionic acid (3aS,5R,6S,6aR)-5-[(R)-1,2-bis-(2,2-dimethyl-propionyloxy)-ethyl]-2-oxo-3-phenylacetyl-hexahydro-furo[2,3-d]oxazol-6-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (3aS,5R,6S,6aR)-5-[(R)-1,2-bis-(2,2-dimethyl-propionyloxy)-ethyl]-2-oxo-3-phenylacetyl-hexahydro-furo[2,3-d]oxazol-6-yl ester(285568-38-9)
EPA Substance Registry System: 2,2-Dimethyl-propionic acid (3aS,5R,6S,6aR)-5-[(R)-1,2-bis-(2,2-dimethyl-propionyloxy)-ethyl]-2-oxo-3-phenylacetyl-hexahydro-furo[2,3-d]oxazol-6-yl ester(285568-38-9)

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: 285568-38-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 285568-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,5,5,6 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 285568-38:
(8*2)+(7*8)+(6*5)+(5*5)+(4*6)+(3*8)+(2*3)+(1*8)=189
189 % 10 = 9
So 285568-38-9 is a valid CAS Registry Number.

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285568-38-9Relevant academic research and scientific papers

New glyco-oxazolidin-2-ones as chiral auxiliaries in boron-mediated asymmetric aldol reactions

Stoever, Michael,Luetzen, Arne,Koell, Peter

, p. 371 - 374 (2000)

Two new chiral glyco-oxazolidin-2-one auxiliaries based on D-glucose are described. Some N-acyl derivatives were synthesized and used in dialkylboron-mediated asymmetric aldol reactions. All reactions delivered as the major diastereomer those predicted by the Zimmerman-Traxler model and were separated by column chromatography and mostly isolated in moderate to good yields. Copyright (C) 2000 Elsevier Science Ltd.

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