Cas 1273048-03-5,(3R,6R,7R,8S,8aR)-6-(tert-butoxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5Hoxazolo[3,2-a]pyridine

1273048-03-5

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Basic information

Product Name: (3R,6R,7R,8S,8aR)-6-(tert-butoxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5Hoxazolo[3,2-a]pyridine
Synonyms: (3R,6R,7R,8S,8aR)-6-(tert-butoxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5Hoxazolo[3,2-a]pyridine
CAS NO:1273048-03-5
Molecular Formula:
Molecular Weight: 502.61
EINECS: N/A
Product Categories: N/A
Mol File: 1273048-03-5.mol
Article Data: 1

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,6R,7R,8S,8aR)-6-(tert-butoxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5Hoxazolo[3,2-a]pyridine(CAS DataBase Reference)
NIST Chemistry Reference: (3R,6R,7R,8S,8aR)-6-(tert-butoxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5Hoxazolo[3,2-a]pyridine(1273048-03-5)
EPA Substance Registry System: (3R,6R,7R,8S,8aR)-6-(tert-butoxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5Hoxazolo[3,2-a]pyridine(1273048-03-5)

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: 1273048-03-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1273048-03-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,3,0,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1273048-03:
(9*1)+(8*2)+(7*7)+(6*3)+(5*0)+(4*4)+(3*8)+(2*0)+(1*3)=135
135 % 10 = 5
So 1273048-03-5 is a valid CAS Registry Number.

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1273048-03-5Relevant articles and documents

Conjugate addition of 2-acetylindole enolates to unsaturated oxazolopiperidone lactams: Enantioselective access to the tetracyclic ring system of ervitsine

Amat, Mercedes,Checa, Begona,Llor, Nuria,Perez, Maria,Bosch, Joan

experimental part, p. 898 - 907 (2011/04/22)

The stereochemical outcomes of the conjugate addition reactions of 2-acetylindole enolates to the unsaturated phenylglycinol-derived oxazolopiperidone lactams 1a-f have been studied. After reduction of the 2-acylindole carbonyl group, the Michael adduct c

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