Cas 162935-66-2,tert-butyl (4S)-4-<(S)-hydroxy<4-benzyloxy-6-(1,3-dioxan-2-yl)-1-(phenylsulfonyl)-1H-indol-2-yl>methyl>-2,2-dimethyloxazolidine-3-carboxylate

162935-66-2

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Basic information

Product Name: tert-butyl (4S)-4-<(S)-hydroxy<4-benzyloxy-6-(1,3-dioxan-2-yl)-1-(phenylsulfonyl)-1H-indol-2-yl>methyl>-2,2-dimethyloxazolidine-3-carboxylate
Synonyms:
CAS NO:162935-66-2
Molecular Formula:
Molecular Weight: 678.803
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: tert-butyl (4S)-4-<(S)-hydroxy<4-benzyloxy-6-(1,3-dioxan-2-yl)-1-(phenylsulfonyl)-1H-indol-2-yl>methyl>-2,2-dimethyloxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (4S)-4-<(S)-hydroxy<4-benzyloxy-6-(1,3-dioxan-2-yl)-1-(phenylsulfonyl)-1H-indol-2-yl>methyl>-2,2-dimethyloxazolidine-3-carboxylate(162935-66-2)
EPA Substance Registry System: tert-butyl (4S)-4-<(S)-hydroxy<4-benzyloxy-6-(1,3-dioxan-2-yl)-1-(phenylsulfonyl)-1H-indol-2-yl>methyl>-2,2-dimethyloxazolidine-3-carboxylate(162935-66-2)

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: 162935-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 162935-66-2 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, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162935-66:
(8*1)+(7*6)+(6*2)+(5*9)+(4*3)+(3*5)+(2*6)+(1*6)=152
152 % 10 = 2
So 162935-66-2 is a valid CAS Registry Number.

162935-66-2Upstream product

102308-32-7 (4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

162935-66-2Downstream Products

162935-66-2Relevant 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 (2007/10/02)

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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