Cas 667422-92-6,1H-Indole-2-carboxylic acid, 5-[4-methoxy-3-(1-methylethyl)phenoxy]-, ethyl ester

667422-92-6

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Basic information

Product Name: 1H-Indole-2-carboxylic acid, 5-[4-methoxy-3-(1-methylethyl)phenoxy]-, ethyl ester
Synonyms:
CAS NO:667422-92-6
Molecular Formula: C21H23NO4
Molecular Weight: 353.418
EINECS: N/A
Product Categories: N/A
Mol File: 667422-92-6.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: 1H-Indole-2-carboxylic acid, 5-[4-methoxy-3-(1-methylethyl)phenoxy]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-2-carboxylic acid, 5-[4-methoxy-3-(1-methylethyl)phenoxy]-, ethyl ester(667422-92-6)
EPA Substance Registry System: 1H-Indole-2-carboxylic acid, 5-[4-methoxy-3-(1-methylethyl)phenoxy]-, ethyl ester(667422-92-6)

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: 667422-92-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 667422-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,7,4,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 667422-92:
(8*6)+(7*6)+(6*7)+(5*4)+(4*2)+(3*2)+(2*9)+(1*2)=186
186 % 10 = 6
So 667422-92-6 is a valid CAS Registry Number.

667422-92-6Upstream product

24985-85-1 ethyl 5-hydroxyindole-2-carboxylate

667422-92-6Downstream Products

667422-93-7 5-(4-hydroxy-3-isopropylphenoxy)-2-carboxyindol ethyl ester

667422-92-6Relevant articles and documents

IDOL DERIVATIVES AS NEW THYROID RECEPTOR AGONIST LIGANDS AND METHODS

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Page 27, (2010/02/05)

This invention relates to novel compounds of the general formula (I), which are thyroid receptor ligands, and are preferably selective for the thyroid hormone receptor Beta and to methods of preparing such compound. In addition, a method is provided for p

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