Cas 156483-03-3,(S)-7-(4-Fluoro-phenyl)-7-(5-hydroxy-6,7-dimethyl-1-oxo-indan-4-yl)-heptanoic acid methyl ester

156483-03-3

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Basic information

Product Name: (S)-7-(4-Fluoro-phenyl)-7-(5-hydroxy-6,7-dimethyl-1-oxo-indan-4-yl)-heptanoic acid methyl ester
Synonyms: (S)-7-(4-Fluoro-phenyl)-7-(5-hydroxy-6,7-dimethyl-1-oxo-indan-4-yl)-heptanoic acid methyl ester
CAS NO:156483-03-3
Molecular Formula:
Molecular Weight: 412.501
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)-7-(4-Fluoro-phenyl)-7-(5-hydroxy-6,7-dimethyl-1-oxo-indan-4-yl)-heptanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-7-(4-Fluoro-phenyl)-7-(5-hydroxy-6,7-dimethyl-1-oxo-indan-4-yl)-heptanoic acid methyl ester(156483-03-3)
EPA Substance Registry System: (S)-7-(4-Fluoro-phenyl)-7-(5-hydroxy-6,7-dimethyl-1-oxo-indan-4-yl)-heptanoic acid methyl ester(156483-03-3)

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: 156483-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 156483-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,4,8 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156483-03:
(8*1)+(7*5)+(6*6)+(5*4)+(4*8)+(3*3)+(2*0)+(1*3)=143
143 % 10 = 3
So 156483-03-3 is a valid CAS Registry Number.

156483-03-3Upstream product

156483-03-3Downstream Products

156483-03-3Relevant academic research and scientific papers

Stereoselective synthesis and thromboxane A2 (TXA2) receptor antagonistic activity of optically active phenol derivatives

Fukumoto, Shoji,Terashita, Zen-Ichi,Ashida, Yasuko,Terao, Shinji,Shiraishi, Mitsuru

, p. 749 - 755 (2007/10/03)

Enantiomers of four potent nonprostanoid thromboxane A2 (TXA2) receptor antagonists, (±)-7-(4-fluorophenyl)-7-(2-hydroxyphenyl)heptanoic acids (1- 4), were synthesized stereoselectively by direct ortho-alkylation of phenols under mod

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