Cas 162935-80-0,(1S,2S)-1-acetoxy-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde

162935-80-0

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Basic information

Product Name: (1S,2S)-1-acetoxy-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde
Synonyms: (1S,2S)-1-acetoxy-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde
CAS NO:162935-80-0
Molecular Formula:
Molecular Weight: 492.529
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: (1S,2S)-1-acetoxy-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S)-1-acetoxy-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde(162935-80-0)
EPA Substance Registry System: (1S,2S)-1-acetoxy-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde(162935-80-0)

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: 162935-80-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 162935-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,3 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 162935-80:
(8*1)+(7*6)+(6*2)+(5*9)+(4*3)+(3*5)+(2*8)+(1*0)=150
150 % 10 = 0
So 162935-80-0 is a valid CAS Registry Number.

162935-80-0Upstream product

68-12-2 N,N-dimethyl-formamide

162935-80-0Downstream Products

162935-81-1 (1S,2S)-8-benzyloxy-2-(tert-butyloxycarbonylamino)-2,3-dihydro-1-hydroxy-1H-pyrrolo<1,2-a>indole-6,9-dicarboxaldehyde

162935-80-0Relevant academic research and scientific papers

Preparation of alkyl-substituted indoles in the benzene portion. Part 13. Enantiospecific synthesis of mitosene analogues related to FR 900482 and FR 66979

Utsunomiya,Muratake,Natsume

, p. 37 - 48 (1995)

An acid-catalyzed indole formation reaction previously reported by us was successfully applied to the preparation of variously substituted 4-hydroxy-1H-indoles 11a-g having carbon and/or heteroatom substituents at the benzene portion of the indole ring, u

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