Cas 73285-89-9,(Z)-7-{(1R,2R,3R,5S)-2-[(E)-(S)-4-(Dimethyl-phenyl-silanyl)-3-hydroxy-but-1-enyl]-3,5-dihydroxy-cyclopentyl}-hept-5-enoic acid methyl ester

73285-89-9

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Basic information

Product Name: (Z)-7-{(1R,2R,3R,5S)-2-[(E)-(S)-4-(Dimethyl-phenyl-silanyl)-3-hydroxy-but-1-enyl]-3,5-dihydroxy-cyclopentyl}-hept-5-enoic acid methyl ester
Synonyms:
CAS NO:73285-89-9
Molecular Formula:
Molecular Weight: 446.659
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)-2-[(E)-(S)-4-(Dimethyl-phenyl-silanyl)-3-hydroxy-but-1-enyl]-3,5-dihydroxy-cyclopentyl}-hept-5-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-7-{(1R,2R,3R,5S)-2-[(E)-(S)-4-(Dimethyl-phenyl-silanyl)-3-hydroxy-but-1-enyl]-3,5-dihydroxy-cyclopentyl}-hept-5-enoic acid methyl ester(73285-89-9)
EPA Substance Registry System: (Z)-7-{(1R,2R,3R,5S)-2-[(E)-(S)-4-(Dimethyl-phenyl-silanyl)-3-hydroxy-but-1-enyl]-3,5-dihydroxy-cyclopentyl}-hept-5-enoic acid methyl ester(73285-89-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 73285-89-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73285-89-9 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, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73285-89:
(7*7)+(6*3)+(5*2)+(4*8)+(3*5)+(2*8)+(1*9)=149
149 % 10 = 9
So 73285-89-9 is a valid CAS Registry Number.

73285-89-9Upstream product

73285-89-9Downstream Products

73285-89-9Relevant 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 (1980)

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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