Cas 74166-49-7,Benzoic acid (3aR,5S,6R,6aR)-1-ethylsulfanyl-6-(2-hydroxy-ethyl)-hexahydro-cyclopenta[c]furan-5-yl ester

74166-49-7

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Basic information

Product Name: Benzoic acid (3aR,5S,6R,6aR)-1-ethylsulfanyl-6-(2-hydroxy-ethyl)-hexahydro-cyclopenta[c]furan-5-yl ester
Synonyms:
CAS NO:74166-49-7
Molecular Formula:
Molecular Weight: 336.452
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: Benzoic acid (3aR,5S,6R,6aR)-1-ethylsulfanyl-6-(2-hydroxy-ethyl)-hexahydro-cyclopenta[c]furan-5-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (3aR,5S,6R,6aR)-1-ethylsulfanyl-6-(2-hydroxy-ethyl)-hexahydro-cyclopenta[c]furan-5-yl ester(74166-49-7)
EPA Substance Registry System: Benzoic acid (3aR,5S,6R,6aR)-1-ethylsulfanyl-6-(2-hydroxy-ethyl)-hexahydro-cyclopenta[c]furan-5-yl ester(74166-49-7)

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: 74166-49-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74166-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,6 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74166-49:
(7*7)+(6*4)+(5*1)+(4*6)+(3*6)+(2*4)+(1*9)=137
137 % 10 = 7
So 74166-49-7 is a valid CAS Registry Number.

74166-49-7Upstream product

74166-49-7Downstream Products

74166-54-4 (Z)-7-{(3R,3aR,4R,5S,6aR)-3-[3-(3-Chloro-phenoxy)-2-hydroxy-propylsulfanyl]-5-hydroxy-hexahydro-cyclopenta[c]furan-4-yl}-hept-5-enoic acid methyl ester

74166-49-7Relevant academic research and scientific papers

SYNTHESIS OF NOVEL PROSTANOIDS HAVING A CYCLOPENTAFURAN STRUCTURE WITH A HEMITHIOACETAL SIDE CHAIN FROM AUCUBIN

Ohno, Kiyotaka,Naruto, Masanobu

, p. 175 - 176 (1980)

The titled prostanoids, methyl (Z)-7-furan-6-yl>-5-heptenoates, were prepared from aucubin via hemithioacetalization in construction of the alkyl-end (C13-C20) side

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