Cas 172320-40-0,(E)-7-{(1R,2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-3-(tert-butyl-dimethyl-silanyloxy)-4-phenoxy-but-1-ynyl]-5-oxo-cyclopentyl}-hept-2-enoic acid isopropylamide

172320-40-0

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Basic information

Product Name: (E)-7-{(1R,2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-3-(tert-butyl-dimethyl-silanyloxy)-4-phenoxy-but-1-ynyl]-5-oxo-cyclopentyl}-hept-2-enoic acid isopropylamide
Synonyms:
CAS NO:172320-40-0
Molecular Formula:
Molecular Weight: 656.066
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: (E)-7-{(1R,2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-3-(tert-butyl-dimethyl-silanyloxy)-4-phenoxy-but-1-ynyl]-5-oxo-cyclopentyl}-hept-2-enoic acid isopropylamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-7-{(1R,2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-3-(tert-butyl-dimethyl-silanyloxy)-4-phenoxy-but-1-ynyl]-5-oxo-cyclopentyl}-hept-2-enoic acid isopropylamide(172320-40-0)
EPA Substance Registry System: (E)-7-{(1R,2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-[(R)-3-(tert-butyl-dimethyl-silanyloxy)-4-phenoxy-but-1-ynyl]-5-oxo-cyclopentyl}-hept-2-enoic acid isopropylamide(172320-40-0)

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: 172320-40-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 172320-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,3,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 172320-40:
(8*1)+(7*7)+(6*2)+(5*3)+(4*2)+(3*0)+(2*4)+(1*0)=100
100 % 10 = 0
So 172320-40-0 is a valid CAS Registry Number.

172320-40-0Upstream product

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172320-40-0Relevant academic research and scientific papers

Synthesis and structure-activity relationships of a new class of selective EP3 receptor agonist, 13,14-didehydro-16-phenoxy analogues of prostaglandin E1

Shimazaki, Youichi,Kameo, Kazuya,Tanami, Tohru,Tanaka, Hideo,Ono, Naoya,Kiuchi, Youichi,Okamoto, Sentaro,Sato, Fumie,Ichikawa, Atsushi

, p. 353 - 362 (2007/10/03)

A series of 13,14-didehydro-16-phenoxy analogues of prostaglandin E1 was synthesized and their agonistic activity on EP receptor subtypes was evaluated. 13,14-Didehydro-16-phenoxy-1-decarboxy analogues, 7e and 7f, display highly selective activity on the EP3 receptor subtype, thus, their utility as a selective anti-ulcer agent can be expected. (C) 2000 Elsevier Science Ltd.

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