Cas 1049705-01-2,(3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

1049705-01-2

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Basic information

Product Name: (3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine
Synonyms: (3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine
CAS NO:1049705-01-2
Molecular Formula:
Molecular Weight: 582.558
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: (3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine(CAS DataBase Reference)
NIST Chemistry Reference: (3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine(1049705-01-2)
EPA Substance Registry System: (3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine(1049705-01-2)

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: 1049705-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1049705-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,7,0 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1049705-01:
(9*1)+(8*0)+(7*4)+(6*9)+(5*7)+(4*0)+(3*5)+(2*0)+(1*1)=142
142 % 10 = 2
So 1049705-01-2 is a valid CAS Registry Number.

1049705-01-2Upstream product

1049705-01-2Downstream Products

1049705-03-4 (3R,8aR)-6-(benzyloxycarbonyl)-5-oxo-3,8a-diphenyl-2,3,8,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine

1049705-01-2Relevant academic research and scientific papers

An enantioselective synthetic route to cis-2,4-disubstituted and 2,4-bridged piperidines

Amat, Mercedes,Perez, Maria,Minaglia, Annamaria T.,Bosch, Joan

, p. 6920 - 6923 (2008/12/22)

(Chemical Equation Presented) A synthetic route to enantiopure cis-2,4-disubstituted and 2,4-bridged piperidines is reported, the key step being a stereoselective conjugate addition of an organocuprate to a phenylglycinol-derived unsaturated lactam bearing a substituent at the 8a-position.

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