Cas 73285-97-9,(Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-((E)-(R)-3-hydroxy-5-oxo-5-phenyl-pent-1-enyl)-cyclopentyl]-hept-5-enoic acid methyl ester

73285-97-9

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Basic information

Product Name: (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-((E)-(R)-3-hydroxy-5-oxo-5-phenyl-pent-1-enyl)-cyclopentyl]-hept-5-enoic acid methyl ester
Synonyms:
CAS NO:73285-97-9
Molecular Formula:
Molecular Weight: 416.514
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: (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-((E)-(R)-3-hydroxy-5-oxo-5-phenyl-pent-1-enyl)-cyclopentyl]-hept-5-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-((E)-(R)-3-hydroxy-5-oxo-5-phenyl-pent-1-enyl)-cyclopentyl]-hept-5-enoic acid methyl ester(73285-97-9)
EPA Substance Registry System: (Z)-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-((E)-(R)-3-hydroxy-5-oxo-5-phenyl-pent-1-enyl)-cyclopentyl]-hept-5-enoic acid methyl ester(73285-97-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 73285-97-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73285-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73285-97:
(7*7)+(6*3)+(5*2)+(4*8)+(3*5)+(2*9)+(1*7)=149
149 % 10 = 9
So 73285-97-9 is a valid CAS Registry Number.

73285-97-9Upstream product

73285-97-9Downstream Products

73285-97-9Relevant academic research and scientific papers

Prostaglandin Analogues Possessing Antinidatory Effects. 1. Modification of the ω Chain

Hayashi, Masaki,Miyake, Hajimu,Kori, Seiji,Tanouchi, Tadao,Wakatsuka, Hirohisa,et al.

, p. 519 - 524 (2007/10/02)

Novel prostaglandin analogues modified in the ω chain were prepared by the reaction of the vinyl aldehydes 1a-e with a variety of organometallic reagents as a key step of the syntheses.Compared with the natural prostaglandin F2α in antinidatory

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