Cas 120386-56-3,Acetic acid 9-benzoylsulfanylmethyl-7-methoxy-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl ester

120386-56-3

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Basic information

Product Name: Acetic acid 9-benzoylsulfanylmethyl-7-methoxy-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl ester
Synonyms:
CAS NO:120386-56-3
Molecular Formula:
Molecular Weight: 425.462
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: Acetic acid 9-benzoylsulfanylmethyl-7-methoxy-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 9-benzoylsulfanylmethyl-7-methoxy-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl ester(120386-56-3)
EPA Substance Registry System: Acetic acid 9-benzoylsulfanylmethyl-7-methoxy-5,8-dioxo-2,3,5,8-tetrahydro-1H-pyrrolo[1,2-a]indol-1-yl ester(120386-56-3)

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: 120386-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120386-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,8 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120386-56:
(8*1)+(7*2)+(6*0)+(5*3)+(4*8)+(3*6)+(2*5)+(1*6)=103
103 % 10 = 3
So 120386-56-3 is a valid CAS Registry Number.

120386-56-3Upstream product

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120386-56-3Relevant academic research and scientific papers

Synthesis, mechanism of action, and biological evaluation of mitosenes

Orlemans,Verboom,Scheltinga,Reinhoudt,Lelieveld,Fiebig,Winterhalter,Double,Bibby

, p. 1612 - 1620 (1989)

Mitosenes of both the pyrrolo- and pyrido[1,2-a]indole type have been prepared via modification of these heterotricyclic compounds. Several mitosenes have been studied for their reactions with nucleophiles under reductive conditions. The results of these

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