Cas 958378-19-3,2-[4-(2-ethoxycarbonylacetyl)phenyl]-2-methylpropionic acid methyl ester

958378-19-3

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Basic information

Product Name: 2-[4-(2-ethoxycarbonylacetyl)phenyl]-2-methylpropionic acid methyl ester
Synonyms: 2-[4-(2-ethoxycarbonylacetyl)phenyl]-2-methylpropionic acid methyl ester
CAS NO:958378-19-3
Molecular Formula:
Molecular Weight: 292.332
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: 2-[4-(2-ethoxycarbonylacetyl)phenyl]-2-methylpropionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[4-(2-ethoxycarbonylacetyl)phenyl]-2-methylpropionic acid methyl ester(958378-19-3)
EPA Substance Registry System: 2-[4-(2-ethoxycarbonylacetyl)phenyl]-2-methylpropionic acid methyl ester(958378-19-3)

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: 958378-19-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 958378-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,3,7 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 958378-19:
(8*9)+(7*5)+(6*8)+(5*3)+(4*7)+(3*8)+(2*1)+(1*9)=233
233 % 10 = 3
So 958378-19-3 is a valid CAS Registry Number.

958378-19-3Upstream product

630385-42-1 methyl 2-(4-chlorocarbonylphenyl)-2-methylpropanoate

958378-19-3Downstream Products

958378-22-8 1-[4-(1-methoxycarbonyl-1-methylethyl)benzoyl]cyclopropane carboxylic acid ethyl ester

958378-19-3Relevant academic research and scientific papers

INTERMEDIATES USEFUL FOR THE PREPARATION OF ANTIHISTAMINIC PIPERIDINE DERIVATIVE

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Page/Page column 12-13; 16, (2008/06/13)

The present invention relates to process for preparing antihistaminic piperidine derivative, specifically fexofenadine and its pharmaceutically acceptable salts by using novel synthetic intermediates of following formula (I), wherein R is lower alkyl; R2 is H, cyclopropyl, R1is alkyl, 4-(hydroxy-dipheτiyl-methyl)-piperidin-l-yl.

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