Cas 146822-74-4,7-{5-[3-(4-Chloro-phenyl)-propionyl]-thiophen-3-yl}-heptanoic acid ethyl ester

146822-74-4

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Basic information

Product Name: 7-{5-[3-(4-Chloro-phenyl)-propionyl]-thiophen-3-yl}-heptanoic acid ethyl ester
Synonyms: 7-{5-[3-(4-Chloro-phenyl)-propionyl]-thiophen-3-yl}-heptanoic acid ethyl ester
CAS NO:146822-74-4
Molecular Formula:
Molecular Weight: 406.974
EINECS: N/A
Product Categories: N/A
Mol File: 146822-74-4.mol
Article Data: 1

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: 7-{5-[3-(4-Chloro-phenyl)-propionyl]-thiophen-3-yl}-heptanoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7-{5-[3-(4-Chloro-phenyl)-propionyl]-thiophen-3-yl}-heptanoic acid ethyl ester(146822-74-4)
EPA Substance Registry System: 7-{5-[3-(4-Chloro-phenyl)-propionyl]-thiophen-3-yl}-heptanoic acid ethyl ester(146822-74-4)

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: 146822-74-4(Hazardous Substances Data)

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146822-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146822-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,8,2 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146822-74:
(8*1)+(7*4)+(6*6)+(5*8)+(4*2)+(3*2)+(2*7)+(1*4)=144
144 % 10 = 4
So 146822-74-4 is a valid CAS Registry Number.

146822-74-4Upstream product

146822-74-4Downstream Products

142422-51-3 7-<5-<3-(4-chlorophenyl)propyl>-3-thienyl>heptanoic acid

146822-74-4Relevant articles and documents

ω-alkanoic Acids: From Specific LTA4 Hydrolase Inhibitors to LTB4 Receptor Antagonists

Labaudiniere, Richard,Hilboll, Gerd,Leon-Lomeli, Alicia,Terlain, Bernard,Cavy, Francoise,et al.

, p. 3170 - 3179 (1992)

A series of ω-alkanoic acid isomers was prepared and a structure-activity relationship was investigated.These compounds have displayed either LTA4 hydrolase inhibition activities or LTB4 receptor binding activities, or both, dependin

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