Cas 196618-04-9,(1R,2R,3S,3aS,4S,6S,7R,7aS)-1,2,3-Tris-benzyloxy-6,7-dihydroxy-octahydro-indene-4-carboxylic acid methyl ester

196618-04-9

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Basic information

Product Name: (1R,2R,3S,3aS,4S,6S,7R,7aS)-1,2,3-Tris-benzyloxy-6,7-dihydroxy-octahydro-indene-4-carboxylic acid methyl ester
Synonyms: (1R,2R,3S,3aS,4S,6S,7R,7aS)-1,2,3-Tris-benzyloxy-6,7-dihydroxy-octahydro-indene-4-carboxylic acid methyl ester
CAS NO:196618-04-9
Molecular Formula:
Molecular Weight: 532.634
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: (1R,2R,3S,3aS,4S,6S,7R,7aS)-1,2,3-Tris-benzyloxy-6,7-dihydroxy-octahydro-indene-4-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3S,3aS,4S,6S,7R,7aS)-1,2,3-Tris-benzyloxy-6,7-dihydroxy-octahydro-indene-4-carboxylic acid methyl ester(196618-04-9)
EPA Substance Registry System: (1R,2R,3S,3aS,4S,6S,7R,7aS)-1,2,3-Tris-benzyloxy-6,7-dihydroxy-octahydro-indene-4-carboxylic acid methyl ester(196618-04-9)

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: 196618-04-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 196618-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,6,1 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 196618-04:
(8*1)+(7*9)+(6*6)+(5*6)+(4*1)+(3*8)+(2*0)+(1*4)=169
169 % 10 = 9
So 196618-04-9 is a valid CAS Registry Number.

196618-04-9Upstream product

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196618-04-9Relevant academic research and scientific papers

Intramolecular Diels-Alder reaction of chiral, highly oxygenated trienoates derived from sugar allytins

Jarosz, Slawomir,Kozlowska, Elzbieta,Jezewski, Artur

, p. 10775 - 10782 (2007/10/03)

The Lewis acid catalyzed intramolecular Diels-Alder reaction of sugar derived trienoates 3 led preferably to bicyclic endo-adducts 4. The best stereoselectivity was observed for cyclization of the L-arabino-trienoate 3b, in which only one isomer (trans) was formed. High pressure (15 kbar) cycloaddition of 3a, 3b, and 3c, led to single stereosiomers 4a, 4b, and 4c in good yields. Conversion of adduct 4a to chiral cyclopentanes was described.

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