Cas 136814-27-2,tert-butyl 7-(2-nitrophenyl)-5,8a-dimethyl-8-methoxycarbonyl-2,3,7,8-tetrahydro-7H-oxazolo<3,2-a>pyridin-6-carboxylate

136814-27-2

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Basic information

Product Name: tert-butyl 7-(2-nitrophenyl)-5,8a-dimethyl-8-methoxycarbonyl-2,3,7,8-tetrahydro-7H-oxazolo<3,2-a>pyridin-6-carboxylate
Synonyms:
CAS NO:136814-27-2
Molecular Formula:
Molecular Weight: 432.474
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: tert-butyl 7-(2-nitrophenyl)-5,8a-dimethyl-8-methoxycarbonyl-2,3,7,8-tetrahydro-7H-oxazolo<3,2-a>pyridin-6-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 7-(2-nitrophenyl)-5,8a-dimethyl-8-methoxycarbonyl-2,3,7,8-tetrahydro-7H-oxazolo<3,2-a>pyridin-6-carboxylate(136814-27-2)
EPA Substance Registry System: tert-butyl 7-(2-nitrophenyl)-5,8a-dimethyl-8-methoxycarbonyl-2,3,7,8-tetrahydro-7H-oxazolo<3,2-a>pyridin-6-carboxylate(136814-27-2)

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: 136814-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136814-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,1 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 136814-27:
(8*1)+(7*3)+(6*6)+(5*8)+(4*1)+(3*4)+(2*2)+(1*7)=132
132 % 10 = 2
So 136814-27-2 is a valid CAS Registry Number.

136814-27-2Upstream product

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136814-27-2Relevant academic research and scientific papers

2,3,8,8a-Tetrahydro-7H-oxazolo[3,2-a]pyridine: A new heterocyclic system

Feliciano, Arturo San,Caballero, Esther,Pereira, Juan A. P.,Puebla, Pilar

, p. 6503 - 6510 (2007/10/02)

Compounds with the previously unreported skeleton of 2,3,8,8a-tetrahydro-7H-oxazolo [3,2-a]pyridine were prepared by reactions between α,β-unsaturated ketones or aldehydes and N-hydroxyethyl-enamines of acetoacetate esters. Other compounds like 1,4-dihydropyridines, aminocyclohexene and cyclohexadiene derivatives were also formed as minor products.

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