Cas 844665-22-1,1-benzyl-3-[N-([2H<sub>5</sub>]ethyl)aniline]-4-(1H-indol-1-yl)-1H-pyrrole-2,5-dione

844665-22-1

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Basic information

Product Name: 1-benzyl-3-[N-([2H₅]ethyl)aniline]-4-(1H-indol-1-yl)-1H-pyrrole-2,5-dione
Synonyms: 1-benzyl-3-[N-([2H₅]ethyl)aniline]-4-(1H-indol-1-yl)-1H-pyrrole-2,5-dione
CAS NO:844665-22-1
Molecular Formula:
Molecular Weight: 426.459
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-benzyl-3-[N-([2H₅]ethyl)aniline]-4-(1H-indol-1-yl)-1H-pyrrole-2,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzyl-3-[N-([2H₅]ethyl)aniline]-4-(1H-indol-1-yl)-1H-pyrrole-2,5-dione(844665-22-1)
EPA Substance Registry System: 1-benzyl-3-[N-([2H₅]ethyl)aniline]-4-(1H-indol-1-yl)-1H-pyrrole-2,5-dione(844665-22-1)

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: 844665-22-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 844665-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,6,6 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 844665-22:
(8*8)+(7*4)+(6*4)+(5*6)+(4*6)+(3*5)+(2*2)+(1*2)=191
191 % 10 = 1
So 844665-22-1 is a valid CAS Registry Number.

844665-22-1Upstream product

844665-22-1Downstream Products

570432-05-2 1,2-dihydro-6-methyl-7-phenyl-9-benzyl-6H-pyrrolo[3',4':2,3][1,4]diazepino[6,7,1-hi]indole-8,10(7H,9H)-dione

844665-22-1Relevant academic research and scientific papers

Diazepines[1,4] annelated with indoline and maleimide from 3-(di)alkylamino-4-(indol-1-yl)maleimides: Mechanism of rearrangement and cyclization

Lakatosh, Sergey A.,Luzikov, Yuri N.,Preobrazhenskaya, Maria N.

, p. 2017 - 2020 (2005)

The mechanism of cyclization of 3-(di)alkylamino-4-(indol-1-yl)maleimides to diazepine[1,4] derivatives was elucidated using deuterium labeled precursors.

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