Cas 182485-96-7,1-(3,4-Diethoxy-phenyl)-8,9-diethoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-2,3-dione

182485-96-7

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Basic information

Product Name: 1-(3,4-Diethoxy-phenyl)-8,9-diethoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-2,3-dione
Synonyms: 1-(3,4-Diethoxy-phenyl)-8,9-diethoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-2,3-dione
CAS NO:182485-96-7
Molecular Formula:
Molecular Weight: 451.519
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: 1-(3,4-Diethoxy-phenyl)-8,9-diethoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-2,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,4-Diethoxy-phenyl)-8,9-diethoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-2,3-dione(182485-96-7)
EPA Substance Registry System: 1-(3,4-Diethoxy-phenyl)-8,9-diethoxy-5,6-dihydro-pyrrolo[2,1-a]isoquinoline-2,3-dione(182485-96-7)

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: 182485-96-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 182485-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,8 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 182485-96:
(8*1)+(7*8)+(6*2)+(5*4)+(4*8)+(3*5)+(2*9)+(1*6)=167
167 % 10 = 7
So 182485-96-7 is a valid CAS Registry Number.

182485-96-7Upstream product

182485-96-7Downstream Products

698994-67-1 C₃₂H₃₃N₃O₄

182485-96-7Relevant academic research and scientific papers

Reactions of 2,3-dioxopyrrolo[2,1-a]isoquinolines with sodium borohydride and the properties of its products

Mikhailovskii

, p. 590 - 595 (1996)

The reaction of 2,3-dioxopyrrolo[2,1-a]isoquinolines with sodium borohydride, depending on the conditions under which it is carried out, can proceed by the route of hydrogenation or by the opening of the pyrrole ring. In the latter case, ketoesters, for which examples of reactions at the dicarbonyl and enamine fragments are presented, are formed. 1996 Plenum Publishing Corporation.

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