Cas 1338700-05-2,(5aR,6R,9aS)-ethyl 6-phenyl-9-tosyl-4,5,5a,6,9.9a-hexahydrothieno[3,2-h]quinoline-8-carboxylate

1338700-05-2

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Basic information

Product Name: (5aR,6R,9aS)-ethyl 6-phenyl-9-tosyl-4,5,5a,6,9.9a-hexahydrothieno[3,2-h]quinoline-8-carboxylate
Synonyms: (5aR,6R,9aS)-ethyl 6-phenyl-9-tosyl-4,5,5a,6,9.9a-hexahydrothieno[3,2-h]quinoline-8-carboxylate
CAS NO:1338700-05-2
Molecular Formula:
Molecular Weight: 493.648
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: (5aR,6R,9aS)-ethyl 6-phenyl-9-tosyl-4,5,5a,6,9.9a-hexahydrothieno[3,2-h]quinoline-8-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (5aR,6R,9aS)-ethyl 6-phenyl-9-tosyl-4,5,5a,6,9.9a-hexahydrothieno[3,2-h]quinoline-8-carboxylate(1338700-05-2)
EPA Substance Registry System: (5aR,6R,9aS)-ethyl 6-phenyl-9-tosyl-4,5,5a,6,9.9a-hexahydrothieno[3,2-h]quinoline-8-carboxylate(1338700-05-2)

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: 1338700-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1338700-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,7,0 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1338700-05:
(9*1)+(8*3)+(7*3)+(6*8)+(5*7)+(4*0)+(3*0)+(2*0)+(1*5)=142
142 % 10 = 2
So 1338700-05-2 is a valid CAS Registry Number.

1338700-05-2Upstream product

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1338700-05-2Relevant academic research and scientific papers

Organocatalytic sequential Hetero-Diels-Alder and Friedel-crafts reaction: Constructions of fused heterocycles with scaffold diversity

Zhou, Si-Li,Li, Jun-Long,Dong, Lin,Chen, Ying-Chun

supporting information; experimental part, p. 5874 - 5877 (2011/12/15)

A highly enantioselective aza-Diels-Alder and Friedel-Crafts reaction sequence of N-sulfonyl-1-aza-1,3-butadienes and aliphatic aldehydes tethered to an arene motif has been developed, affording the fused chiral piperidine frameworks with a versatile scaf

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