Cas 145274-50-6,2-(2-Amino-3-carbamoyl-5,7a-dihydro-7a-methyl-5-oxo-1-phenyl-1H-indol-4-yl)-2-butendicarbonsaeuredimethylester

145274-50-6

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Basic information

Product Name: 2-(2-Amino-3-carbamoyl-5,7a-dihydro-7a-methyl-5-oxo-1-phenyl-1H-indol-4-yl)-2-butendicarbonsaeuredimethylester
Synonyms:
CAS NO:145274-50-6
Molecular Formula:
Molecular Weight: 423.425
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-(2-Amino-3-carbamoyl-5,7a-dihydro-7a-methyl-5-oxo-1-phenyl-1H-indol-4-yl)-2-butendicarbonsaeuredimethylester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-Amino-3-carbamoyl-5,7a-dihydro-7a-methyl-5-oxo-1-phenyl-1H-indol-4-yl)-2-butendicarbonsaeuredimethylester(145274-50-6)
EPA Substance Registry System: 2-(2-Amino-3-carbamoyl-5,7a-dihydro-7a-methyl-5-oxo-1-phenyl-1H-indol-4-yl)-2-butendicarbonsaeuredimethylester(145274-50-6)

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: 145274-50-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145274-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,7 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 145274-50:
(8*1)+(7*4)+(6*5)+(5*2)+(4*7)+(3*4)+(2*5)+(1*0)=126
126 % 10 = 6
So 145274-50-6 is a valid CAS Registry Number.

145274-50-6Upstream product

145274-50-6Downstream Products

145256-67-3 1-Carbamoyl-3a,7-dihydro-2-imino-3a-methyl-7-oxo-1-phenyl-2H-pyrano<3,2-e>indol

145274-50-6Relevant academic research and scientific papers

2-Amino-3-cyano-dihydroindol-5-ones, III: Reports on the chemical reactivity of a new class of compounds

Eger,Frey

, p. 551 - 556 (1992)

The chemical reactivity of cytotoxic 5-indolone derivatives is examined in order to get ideas about their behaviour in biological systems. Dienone-phenol-rearrangement preserving the indole ring system could not be achieved, aromatization of 1b gives the

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