Cas 1586818-95-2,methyl 3-(4-bromobenzoyl)-4-hydroxy-2-(2-methyl-1H-indol-3-yl)-5-oxo-1-(4-tolyl)-2,5-dihydro-1-pyrrole-2-carboxylate

1586818-95-2

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Basic information

Product Name: methyl 3-(4-bromobenzoyl)-4-hydroxy-2-(2-methyl-1H-indol-3-yl)-5-oxo-1-(4-tolyl)-2,5-dihydro-1-pyrrole-2-carboxylate
Synonyms:
CAS NO:1586818-95-2
Molecular Formula:
Molecular Weight: 559.416
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: methyl 3-(4-bromobenzoyl)-4-hydroxy-2-(2-methyl-1H-indol-3-yl)-5-oxo-1-(4-tolyl)-2,5-dihydro-1-pyrrole-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3-(4-bromobenzoyl)-4-hydroxy-2-(2-methyl-1H-indol-3-yl)-5-oxo-1-(4-tolyl)-2,5-dihydro-1-pyrrole-2-carboxylate(1586818-95-2)
EPA Substance Registry System: methyl 3-(4-bromobenzoyl)-4-hydroxy-2-(2-methyl-1H-indol-3-yl)-5-oxo-1-(4-tolyl)-2,5-dihydro-1-pyrrole-2-carboxylate(1586818-95-2)

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: 1586818-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1586818-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,6,8,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1586818-95:
(9*1)+(8*5)+(7*8)+(6*6)+(5*8)+(4*1)+(3*8)+(2*9)+(1*5)=232
232 % 10 = 2
So 1586818-95-2 is a valid CAS Registry Number.

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1586818-95-2Relevant academic research and scientific papers

Five-membered dioxoheterocycles: XCIX. Reaction of 1-aryl-4-aroyl-5- methoxycarbonyl-1H-pyrrole-2,3-diones with indoles. Crystal and molecular structure of substituted 2-(indol-3-yl)pyrrole

Denislamova,Slepukhin,Maslivets

, (2014)

1-Aryl-4-aroyl-5-methoxycarbonyl-1H-pyrrole-2,3-diones react with indole and 2-methylindole with the formation of methyl 1-aryl-3-aroyl-4-hydroxy-2-(1H- indol-3-yl)-5-oxo-2,5-dihydro-1H-pyrrole-2-carboxylates. Crystal and molecular structure of methyl 3-b

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