Cas 1309455-16-0,(5S,8aR)-5-benzyl-7-cyclopentyl-8,8a-dihydro-1H-oxazolo[3,4-a]pyrazine-3,6(5H,7H)-dione

1309455-16-0

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Basic information

Product Name: (5S,8aR)-5-benzyl-7-cyclopentyl-8,8a-dihydro-1H-oxazolo[3,4-a]pyrazine-3,6(5H,7H)-dione
Synonyms: (5S,8aR)-5-benzyl-7-cyclopentyl-8,8a-dihydro-1H-oxazolo[3,4-a]pyrazine-3,6(5H,7H)-dione
CAS NO:1309455-16-0
Molecular Formula:
Molecular Weight: 314.384
EINECS: N/A
Product Categories: N/A
Mol File: 1309455-16-0.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: (5S,8aR)-5-benzyl-7-cyclopentyl-8,8a-dihydro-1H-oxazolo[3,4-a]pyrazine-3,6(5H,7H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: (5S,8aR)-5-benzyl-7-cyclopentyl-8,8a-dihydro-1H-oxazolo[3,4-a]pyrazine-3,6(5H,7H)-dione(1309455-16-0)
EPA Substance Registry System: (5S,8aR)-5-benzyl-7-cyclopentyl-8,8a-dihydro-1H-oxazolo[3,4-a]pyrazine-3,6(5H,7H)-dione(1309455-16-0)

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: 1309455-16-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309455-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,4,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1309455-16:
(9*1)+(8*3)+(7*0)+(6*9)+(5*4)+(4*5)+(3*5)+(2*1)+(1*6)=150
150 % 10 = 0
So 1309455-16-0 is a valid CAS Registry Number.

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1309455-16-0Relevant articles and documents

Intramolecular palladium-catalyzed aminocarboxylation of olefins as a direct route to bicyclic oxazolidinones

Borsini, Elena,Broggini, Gianluigi,Fasana, Andrea,Galli, Simona,Khansaa, Maisaa,Piarulli, Umberto,Rigamonti, Micol

, p. 985 - 994 (2011/06/19)

An efficient, direct synthesis of oxazolidinones fused to six-membered heterocyclic rings starting from carbamate-protected aminoalkenes has been developed. This procedure is based on an oxidative palladium(II)-catalyzed reaction performed in the presence

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