Cas 676441-73-9,(S)-3-((13R,14R,17S,18S)-13-Hydroxy-14,17,18-tris-methoxymethoxy-triacontyl)-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one

676441-73-9

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Basic information

Product Name: (S)-3-((13R,14R,17S,18S)-13-Hydroxy-14,17,18-tris-methoxymethoxy-triacontyl)-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one
Synonyms: (S)-3-((13R,14R,17S,18S)-13-Hydroxy-14,17,18-tris-methoxymethoxy-triacontyl)-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one
CAS NO:676441-73-9
Molecular Formula:
Molecular Weight: 825.245
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: (S)-3-((13R,14R,17S,18S)-13-Hydroxy-14,17,18-tris-methoxymethoxy-triacontyl)-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((13R,14R,17S,18S)-13-Hydroxy-14,17,18-tris-methoxymethoxy-triacontyl)-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one(676441-73-9)
EPA Substance Registry System: (S)-3-((13R,14R,17S,18S)-13-Hydroxy-14,17,18-tris-methoxymethoxy-triacontyl)-5-methyl-3-phenylsulfanyl-dihydro-furan-2-one(676441-73-9)

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: 676441-73-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 676441-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,4 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 676441-73:
(8*6)+(7*7)+(6*6)+(5*4)+(4*4)+(3*1)+(2*7)+(1*3)=189
189 % 10 = 9
So 676441-73-9 is a valid CAS Registry Number.

676441-73-9Upstream product

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676441-73-9Relevant academic research and scientific papers

Synthesis and mitochondrial complex I inhibition of dihydroxy-cohibin A, non-THF annonaceous acetogenin analogue

Konno, Hiroyuki,Hiura, Naoki,Makabe, Hidefumi,Abe, Masato,Miyoshi, Hideto

, p. 629 - 632 (2007/10/03)

To elucidate the inhibitory action of acetogenins, we synthesized an acetogenin derivative which possesses tetraol in place of the tetrahydrofuran ring and examined its inhibitory activity against bovine heart mitochondrial complex I. Our results indicate that these hydroxy groups are an essential structural factor though it is not effective as bis-THF hydroxy groups combination.

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