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Ethyl 4-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl-alpha,alpha-dimethylbenzeneacetate hydrochloride is a complex organic hydrochloride salt featuring a piperidine ring and a benzene ring, with additional ethyl, hydroxydiphenylmethyl, and alpha,alpha-dimethylbenzeneacetate groups. This chemical compound holds potential for pharmaceutical applications due to its intricate molecular structure, which may confer specific molecular targets and mechanisms of action within biological systems.

76811-96-6

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76811-96-6 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 4-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl-alpha,alpha-dimethylbenzeneacetate hydrochloride is used as a potential therapeutic agent for the treatment of certain medical conditions. Its unique structure suggests it may interact with specific biological targets, offering new avenues for drug development and treatment strategies.
Ethyl 4-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl-alpha,alpha-dimethylbenzeneacetate hydrochloride's exact applications and mechanisms of action would require further research to establish its safety, efficacy, and optimal use in medical treatments. As with any new pharmaceutical candidate, extensive testing and clinical trials would be necessary to validate its potential benefits and to understand any possible side effects or contraindications.

Check Digit Verification of cas no

The CAS Registry Mumber 76811-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,1 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76811-96:
(7*7)+(6*6)+(5*8)+(4*1)+(3*1)+(2*9)+(1*6)=156
156 % 10 = 6
So 76811-96-6 is a valid CAS Registry Number.
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

76811-96-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[4-[4-[4-[hydroxy(diphenyl)methyl]piperidin-1-yl]butanoyl]phenyl]-2-methylpropanoate,hydrochloride

1.2 Other means of identification

Product number -
Other names O879

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76811-96-6 SDS

76811-96-6Downstream Products

76811-96-6Relevant academic research and scientific papers

ANTIHISTAMINIC PIPERIDINE DERIVATIVES AND INTERMEDIATES FOR THE PREPARATION THEREOF

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Page/Page column 30, (2010/11/03)

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

-

, (2008/06/13)

This invention relates to novel piperidine derivatives of formula (I) and a process for the preparation thereof. wherein R1is H or C1-C6alkyl wherein the C1-C6alkyl moiety is straight or branched; R2is —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

-

, (2008/06/13)

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.

Intermediates useful for the preparation of antihistaminic piperidine derivatives

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Page column 103, (2010/01/30)

The present invention is related to a novel intermediates and processes which are useful in the preparation of certain antihistaminic piperidine derivatives of the formula whereinW represents —C(=O)— or —CH(OH)—;R1 represents hydrogen or hydroxy;R2 represents hydrogen;R1 and R2 taken together form a second bond between the carbon atoms bearing R1 and R2;n is an integer of from 1 to 5;m is an integer 0 or 1;R3 is —COOH or —COOalkyl wherein the alkyl moiety has from 1 to 6 carbon atoms and is straight or branched each of A is hydrogen or hydroxy; and pharmaceutically acceptable salts and individual optical isomers thereof,with the proviso that where R1 and R2 are taken together to form a second bond between the carbon atoms bearing R1 and R2 or where R1 represented hydroxy, m is an integer 0.

Antihistaminic piperidine derivatives and intermediates for the preparation thereof

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Page column 25, (2010/02/05)

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.

Piperidine derivatives

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, (2008/06/13)

Pharmaceutically useful compounds of the following formula: STR1 wherein R1 represents hydrogen or hydroxy; R2 represents hydrogen; or R1 and R2 taken together form a second bond between the carbon atoms bearing R1 and R2 ; n is a positive whole integer of from 1 to 5; R3 is --CH3, --CH2 OH, --COOH or --COOalkyl wherein the alkyl moiety has from 1 to 6 carbon atoms and is straight or branched; and A and B are individually hydrogen or hydroxy; with the provisos that at least one of A or B is hydrogen and one of A or B is other than hydrogen when R3 is --CH3 ; and pharmaceutically acceptable acid addition salts thereof.

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