Cas 75608-77-4,5-((3aR,6aS)-3-Phenylsulfanyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-2-yl)-pentanoic acid methyl ester

75608-77-4

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Basic information

Product Name: 5-((3aR,6aS)-3-Phenylsulfanyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-2-yl)-pentanoic acid methyl ester
Synonyms:
CAS NO:75608-77-4
Molecular Formula:
Molecular Weight: 332.464
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: 5-((3aR,6aS)-3-Phenylsulfanyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-2-yl)-pentanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-((3aR,6aS)-3-Phenylsulfanyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-2-yl)-pentanoic acid methyl ester(75608-77-4)
EPA Substance Registry System: 5-((3aR,6aS)-3-Phenylsulfanyl-4,5,6,6a-tetrahydro-3aH-cyclopenta[b]furan-2-yl)-pentanoic acid methyl ester(75608-77-4)

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: 75608-77-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75608-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,0 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75608-77:
(7*7)+(6*5)+(5*6)+(4*0)+(3*8)+(2*7)+(1*7)=154
154 % 10 = 4
So 75608-77-4 is a valid CAS Registry Number.

75608-77-4Upstream product

75608-77-4Downstream Products

75608-77-4Relevant academic research and scientific papers

Reaction of prostacyclin methyl ester with benzenesulfenyl chloride preparation of stable prostacyclin analogs

Toru, Takeshi,Watanabe, Kenzo,Oba, Takeo,Tanaka, Toshio,Okamura, Noriaki,Bannai, Kiyoshi,Kurozumi, Seizi

, p. 2539 - 2542 (2007/10/02)

Several phenyl sulfides including stable 5- and 7-phenylthioprostacyclins were obtained by the reaction of the vinyl ether (1) and prostacyclin methyl ester (5) with PhSCl.

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