Cas 176982-87-9,2-(4-Benzyloxy-3,5-dimethoxy-phenyl)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-2-morpholin-4-yl-hexanenitrile

176982-87-9

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Basic information

Product Name: 2-(4-Benzyloxy-3,5-dimethoxy-phenyl)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-2-morpholin-4-yl-hexanenitrile
Synonyms: 2-(4-Benzyloxy-3,5-dimethoxy-phenyl)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-2-morpholin-4-yl-hexanenitrile
CAS NO:176982-87-9
Molecular Formula:
Molecular Weight: 585.657
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: 2-(4-Benzyloxy-3,5-dimethoxy-phenyl)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-2-morpholin-4-yl-hexanenitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-Benzyloxy-3,5-dimethoxy-phenyl)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-2-morpholin-4-yl-hexanenitrile(176982-87-9)
EPA Substance Registry System: 2-(4-Benzyloxy-3,5-dimethoxy-phenyl)-6-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-2-morpholin-4-yl-hexanenitrile(176982-87-9)

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: 176982-87-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176982-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,9,8 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 176982-87:
(8*1)+(7*7)+(6*6)+(5*9)+(4*8)+(3*2)+(2*8)+(1*7)=199
199 % 10 = 9
So 176982-87-9 is a valid CAS Registry Number.

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176982-87-9Relevant academic research and scientific papers

A novel synthesis of piperidin-3-ones via an intramolecular Amadori-type reaction

Guzi, Timothy J.,Macdonald, Timothy L.

, p. 2939 - 2942 (2007/10/03)

1-Methoxycarbonyl-2-(3,5-dimethoxy-4-benzyloxyphenyl)-piperidin-3 one 1 and rac-5R, 8aS-5-(3,5-dimethoxy-4-t-butyldimethylsiloxyphenyl)-oxazolo[3,4:1,6]-p iperidin-3,6-dione 2 were synthesized via an intramolecular adaptation of the biochemically well-characterized Amadori reaction.

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