Cas 1620329-22-7,(7S,9R,10aS)-7-(2-hydroxyethyl)-8,8-dimethyl-9-phenyl-8,9,10,10a-tetrahydro-7H-benzo[4,5]isothiazolo[2,3-a]pyridine 5,5-dioxide

1620329-22-7

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Basic information

Product Name: (7S,9R,10aS)-7-(2-hydroxyethyl)-8,8-dimethyl-9-phenyl-8,9,10,10a-tetrahydro-7H-benzo[4,5]isothiazolo[2,3-a]pyridine 5,5-dioxide
Synonyms: (7S,9R,10aS)-7-(2-hydroxyethyl)-8,8-dimethyl-9-phenyl-8,9,10,10a-tetrahydro-7H-benzo[4,5]isothiazolo[2,3-a]pyridine 5,5-dioxide
CAS NO:1620329-22-7
Molecular Formula:
Molecular Weight: 371.5
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: (7S,9R,10aS)-7-(2-hydroxyethyl)-8,8-dimethyl-9-phenyl-8,9,10,10a-tetrahydro-7H-benzo[4,5]isothiazolo[2,3-a]pyridine 5,5-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: (7S,9R,10aS)-7-(2-hydroxyethyl)-8,8-dimethyl-9-phenyl-8,9,10,10a-tetrahydro-7H-benzo[4,5]isothiazolo[2,3-a]pyridine 5,5-dioxide(1620329-22-7)
EPA Substance Registry System: (7S,9R,10aS)-7-(2-hydroxyethyl)-8,8-dimethyl-9-phenyl-8,9,10,10a-tetrahydro-7H-benzo[4,5]isothiazolo[2,3-a]pyridine 5,5-dioxide(1620329-22-7)

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: 1620329-22-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620329-22-7 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, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1620329-22:
(9*1)+(8*6)+(7*2)+(6*0)+(5*3)+(4*2)+(3*9)+(2*2)+(1*2)=127
127 % 10 = 7
So 1620329-22-7 is a valid CAS Registry Number.

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1620329-22-7Relevant 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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