Cas 1620329-19-2,((3aS,4R,11aS)-10,10-dioxido-4-phenyl-1,3a,4,11a-tetrahydrobenzo[4,5]isothiazolo[2,3-a]cyclopenta[e]pyridin-3-yl)(phenyl)methanone

1620329-19-2

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Basic information

Product Name: ((3aS,4R,11aS)-10,10-dioxido-4-phenyl-1,3a,4,11a-tetrahydrobenzo[4,5]isothiazolo[2,3-a]cyclopenta[e]pyridin-3-yl)(phenyl)methanone
Synonyms: ((3aS,4R,11aS)-10,10-dioxido-4-phenyl-1,3a,4,11a-tetrahydrobenzo[4,5]isothiazolo[2,3-a]cyclopenta[e]pyridin-3-yl)(phenyl)methanone
CAS NO:1620329-19-2
Molecular Formula:
Molecular Weight: 439.535
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: ((3aS,4R,11aS)-10,10-dioxido-4-phenyl-1,3a,4,11a-tetrahydrobenzo[4,5]isothiazolo[2,3-a]cyclopenta[e]pyridin-3-yl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: ((3aS,4R,11aS)-10,10-dioxido-4-phenyl-1,3a,4,11a-tetrahydrobenzo[4,5]isothiazolo[2,3-a]cyclopenta[e]pyridin-3-yl)(phenyl)methanone(1620329-19-2)
EPA Substance Registry System: ((3aS,4R,11aS)-10,10-dioxido-4-phenyl-1,3a,4,11a-tetrahydrobenzo[4,5]isothiazolo[2,3-a]cyclopenta[e]pyridin-3-yl)(phenyl)methanone(1620329-19-2)

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: 1620329-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620329-19-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,3,2 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1620329-19:
(9*1)+(8*6)+(7*2)+(6*0)+(5*3)+(4*2)+(3*9)+(2*1)+(1*9)=132
132 % 10 = 2
So 1620329-19-2 is a valid CAS Registry Number.

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1620329-19-2Relevant academic research and scientific papers

β,γ-regioselective inverse-electron-demand aza-Diels?Alder reactions with α,β-unsaturated aldehydes via dienamine catalysis

Gu, Jing,Ma, Chao,Li, Qing-Zhu,Du, Wei,Chen, Ying-Chun

supporting information, p. 3986 - 3989 (2014/08/18)

A stereoselective inverse-electron-demand aza-Diels-Alder cycloaddition process of cyclic 1-aza-1,3-butadienes and α,β-unsaturated aldehydes has been developed via dienamine catalysis. This reaction exhibits excellent β,γ- regioselectivity for enal substr

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