76811-96-6

Basic information

• Product Name: Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride
• Synonyms: ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride;ETHYL,4-(4-[HYDROXYDIPHENYLMETHYL-1-PIPERIDINYL]-1-OXBUTYL)-A,A DIMETHYLBENZENE ACETATE HCL;ETHYL-4-(4-[HYDROXYDIPHENYLMETHYL-1-PIPERIDINYL]-1-OXBUTYL)-A,A DIMETHYLBENZENE ACETATE HYDROCHLORIDE;4-[4-[4-(HYDROXYDIPHENYLMETHYL)-1-PIPERIDINYL]-1-OXOBUTYL]-A,A-DIMETHYL-BENZENEACETIC ACID ETHYL ESTER, HYDROCHLORIDE;Ethyl 4-{4-[4-(Hydroxydiphenylmethyl)-1-Piperidinyl]-1-Oxobutyl}--Dimethylben;Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-α,α-dimethylbenzeneacetate, hydrochloride;ETHYL 4-{4-4-(HYDROXYDIPHENYLMETHYL)-1-PIPERIDINYL-1-OXOBUTYL}-ALPHA,ALPHA-DIMETHYLBENZENEACETATE HCL;Ethyl 4--alpha,alpha-dimethylbenzeneacetate hydrochloride
• CAS NO: 76811-96-6
• Molecular Formula: C34H42ClNO4
• Molecular Weight: 564.15
• Mol File: 76811-96-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 686.1 °C at 760 mmHg
• Flash Point: 368.8 °C
• Appearance: /
• Vapor Pressure: 9.07E-20mmHg at 25°C
• CAS DataBase Reference: Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride(76811-96-6)
• EPA Substance Registry System: Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride(76811-96-6)

Safety Data

• Hazardous Substances Data: 76811-96-6(Hazardous Substances Data)

Usage

General Description

Ethyl 4-{4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl}-alpha,alpha-dimethylbenzeneacetate hydrochloride is a chemical compound with potential pharmaceutical applications. It is a hydrochloride salt that contains a piperidine ring and a benzene ring, with ethyl, hydroxydiphenylmethyl, and alpha,alpha-dimethylbenzeneacetate groups attached. The compound may have properties that make it suitable for use in the treatment of certain medical conditions, although further research is likely needed to establish its safety and efficacy. Its complex structure suggests it may have specific molecular targets and mechanisms of action within the body, potentially making it a candidate for drug development efforts.

InChI:InChI=1/C34H41NO4.ClH/c1-4-39-32(37)33(2,3)27-19-17-26(18-20-27)31(36)16-11-23-35-24-21-30(22-25-35)34(38,28-12-7-5-8-13-28)29-14-9-6-10-15-29;/h5-10,12-15,17-20,30,38H,4,11,16,21-25H2,1-3H3;1H

Upstream product

• 76811-97-7 4-(4-chloro-1-oxobutyl)-α,α-dimethylbenzeneacetic acid ethyl ester 
• 115-46-8 C₁₈H₂₁NO 

Relevant articles and documents

ANTIHISTAMINIC PIPERIDINE DERIVATIVES AND INTERMEDIATES FOR THE PREPARATION THEREOF

This invention relates to novel piperidine derivatives of formula (I) and a process for the preparation thereof, wherein R1 is H or C1-C6alkyl wherein the C1-C6alkyl moiety is straight or branched; R2 is -COOH or -COOalkyl wherein the alkyl moiety has from 1 to 6 carbon atoms and is straight or branched; or stereoisomers or pharmaceutically acceptable acid addition salt thereof.

Novel antihistaminic piperidine derivatives and intermediates for the preparation thereof

This invention relates to novel piperidine derivatives of formula (I) and a process for the preparation thereof. wherein R1 is H or C1-C6alkyl wherein the C1-C6alkyl moiety is straight or branched; R2 is —COOH or —COOalkyl wherein the alkyl moiety has from 1 to 6 carbon atoms and is straight or branched; or stereoisomers or pharmaceutically acceptable acid addition salt thereof.

Antihistaminic piperidine derivatives and intermediates for the preparation thereof

This invention relates to novel piperidine derivatives of formula (I) and a process for the preparation thereof.whereinR1 is H or C1-C6alkyl wherein the C1-C6alkyl moiety is straight or branched;R2 is -COOH or -COOalkyl wherein the alkyl moiety has from 1 to 6 carbon atoms and is straight or branched; orstereoisomers or pharmaceutically acceptable acid addition salt thereof.