Cas 79562-61-1,Benzyl 2,3-Dihydro-8-hydroxy-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate

79562-61-1

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Basic information

Product Name: Benzyl 2,3-Dihydro-8-hydroxy-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate
Synonyms:
CAS NO:79562-61-1
Molecular Formula:
Molecular Weight: 445.493
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: Benzyl 2,3-Dihydro-8-hydroxy-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: Benzyl 2,3-Dihydro-8-hydroxy-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate(79562-61-1)
EPA Substance Registry System: Benzyl 2,3-Dihydro-8-hydroxy-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate(79562-61-1)

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: 79562-61-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79562-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,6 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79562-61:
(7*7)+(6*9)+(5*5)+(4*6)+(3*2)+(2*6)+(1*1)=171
171 % 10 = 1
So 79562-61-1 is a valid CAS Registry Number.

79562-61-1Upstream product

79562-60-0 Benzyl 2,3,5,6,7,8-Hexahydro-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-8-oxo-1H-pyrrolo<1,2-a>indole-9-carboxylate

79562-61-1Downstream Products

79562-61-1Relevant academic research and scientific papers

Total Synthesis of a Mitosene

Rebek, Julius,Shaber, Steven H.,Shue, Youe-Kong,Gehret, Jean-Claude,Zimmerman, Stephen

, p. 5164 - 5174 (2007/10/02)

The total synthesis of a mitosene (a chemical degradation product of mitomycin C) is described.The synthesis begins with hydroxyproline and uses a Huisgen pyrrole synthesis to form a pyrrolizidine system.The carbocyclic ring is made through Dieckmann cycl

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