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4-(2,6-Dimethyl-piperidin-1-ylmethyl)-phenylamine, an organic amine with the molecular formula C17H27N, is a chemical compound featuring a piperidine ring and a phenyl group. It is recognized for its potential medicinal properties and serves as a crucial building block in the synthesis of various pharmaceuticals and organic compounds. The presence of the piperidine ring in its structure indicates possible biological activity, making it a significant chemical intermediate in drug discovery and development.

328289-91-4

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328289-91-4 Usage

Uses

Used in Pharmaceutical Industry:
4-(2,6-Dimethyl-piperidin-1-ylmethyl)-phenylamine is used as a chemical intermediate for the synthesis of various pharmaceuticals and organic compounds. Its unique structure with a piperidine ring and phenyl group contributes to the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry Research:
4-(2,6-Dimethyl-piperidin-1-ylmethyl)-phenylamine is used as a research compound in medicinal chemistry for exploring its potential as an anticancer and antiviral agent. Its biological activity, attributed to the presence of the piperidine ring, is of interest to scientists working on drug discovery and development.
Used in Drug Synthesis:
4-(2,6-Dimethyl-piperidin-1-ylmethyl)-phenylamine is used as a key component in the synthesis of drugs with potential therapeutic benefits. Its versatile structure allows for the creation of various drug candidates that can be further optimized for improved efficacy and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 328289-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,2,8 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 328289-91:
(8*3)+(7*2)+(6*8)+(5*2)+(4*8)+(3*9)+(2*9)+(1*1)=174
174 % 10 = 4
So 328289-91-4 is a valid CAS Registry Number.

328289-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2,6-dimethylpiperidin-1-yl)methyl]aniline

1.2 Other means of identification

Product number -
Other names 4-[(2,6-dimethylpiperidyl)methyl]phenylamine

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:328289-91-4 SDS

328289-91-4Upstream product

328289-91-4Downstream Products

328289-91-4Relevant academic research and scientific papers

BETA-KETOAMIDE COMPOUNDS HAVING AN MCH-ANTAGONISTIC EFFECT AND MEDICAMENTS CONTAINING SAID COMPOUNDS

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Page/Page column 80, (2008/06/13)

The invention relates to β-ketoamide compounds of general formula (I) wherein the groups and radicals A, B, b, X, Y, Z, R1, R2, R3, R5a and R5b have the designations cited in patent claim 1. The invention also relates to medicaments containing at least one inventive amide. As a result of the MCH receptor antagonistic activity, the inventive medicaments are suitable for treating metabolic disorders and/or eating disorders, especially adipositas, bulimia, anorexia, hyperphagia and diabetes.

Beta-ketoamide compounds with MCH antagonistic activity

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Page/Page column 80, (2008/06/13)

Compounds of formula I wherein the groups and residues A, B, b, X, Y, Z, R1, R2, R3, R5a and R5b have the meanings given in claim 1. The invention further relates to pharmaceutical compositions containing at least one amide according to the invention. As a result of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia, and diabetes.

Substituted indolinones, preparation thereof and their use as pharmaceutical compositions

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, (2008/06/13)

Indolinones of general formula I which are inhibitors of cell proliferation, particularly of tumour cells, and inhibitors of protein kinases. The following compounds are exemplary: (Z)-3-{1-[4-(N-(2-aminoethyl)-N-methylsulphonyl-amino)-phenylamino]-1-phenyl-methylidene}-5-phenylsulphonylamino-2-indolinone, (Z)-3-{1 -[4-(N-(2-dimethylaminoethyl)-N-phenylsulphonyl-amino)-phenylamino]-1-phenyl-methylidene}-5-phenylsulphonylamino-2-indolinone, and (Z)-3-{1-[4-(4-methylpiperazinomethyl)-phenylamino]-1-phenyl-methylidene}-5-phenylsulphonylamino-2-indolinone.

Substituted indolinones with kinase inhibitory activity

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, (2008/06/13)

Substituted indolinones of general formula having effect on various kinases and cycline/CDK complexes and on the proliferation of various tumour cells. Exemplary compounds are: 3-Z-[1-(4-(N-Benzyl-N-methyl-aminomethyl)-phenylamino)-1-methyl-methylene]-5-a

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