Cas 93528-75-7,Benzyl 2,3-Dihydro-8-hydroxy-2-<(methylsulfonyl)oxy>-1-methoxy-6-methyl-1H-pyrrolo<1,2-a>indole-9-carboxylate

93528-75-7

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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:93528-75-7
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(93528-75-7)
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(93528-75-7)

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: 93528-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93528-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,2 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93528-75:
(7*9)+(6*3)+(5*5)+(4*2)+(3*8)+(2*7)+(1*5)=157
157 % 10 = 7
So 93528-75-7 is a valid CAS Registry Number.

93528-75-7Upstream 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

93528-75-7Downstream Products

93528-75-7Relevant 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 (1984)

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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