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4-(1H-Imidazol-1-ylmethyl)-piperidine is a chemical compound characterized by the molecular formula C11H18N2. It is a derivative of piperidine with an imidazole ring attached to one of its carbon atoms, which endows it with unique structural and functional properties. 4-(1H-IMIDAZOL-1-YLMETHYL)-PIPERIDINE is recognized for its role as a versatile building block in organic synthesis and pharmaceutical research, particularly due to the presence of the imidazole moiety, which is a key structural element in many biologically active molecules and pharmaceuticals.

90748-03-1

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90748-03-1 Usage

Uses

Used in Medicinal Chemistry:
4-(1H-Imidazol-1-ylmethyl)-piperidine is used as a key intermediate in the synthesis of biologically active molecules and pharmaceuticals. Its unique structure allows for the development of compounds with potential therapeutic applications, making it a valuable asset in the field of medicinal chemistry.
Used in Drug Discovery:
In the realm of drug discovery, 4-(1H-Imidazol-1-ylmethyl)-piperidine serves as a crucial component in the design and synthesis of new drugs. Its presence in a molecule can influence pharmacokinetic and pharmacodynamic properties, contributing to the discovery of novel therapeutic agents.
Used in Organic Synthesis:
4-(1H-Imidazol-1-ylmethyl)-piperidine is utilized as a building block in organic synthesis, where it can be incorporated into a wide range of chemical structures. This versatility makes it suitable for the creation of complex organic compounds for various applications, including but not limited to pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Research:
In pharmaceutical research, 4-(1H-Imidazol-1-ylmethyl)-piperidine is employed to explore its potential in the development of new drugs and bioactive compounds. Its unique structural features make it an attractive candidate for the creation of molecules with specific biological activities, which can be further optimized for therapeutic use.

Check Digit Verification of cas no

The CAS Registry Mumber 90748-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90748-03:
(7*9)+(6*0)+(5*7)+(4*4)+(3*8)+(2*0)+(1*3)=141
141 % 10 = 1
So 90748-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H15N3/c1-3-10-4-2-9(1)7-12-6-5-11-8-12/h5-6,8-10H,1-4,7H2

90748-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1H-imidazol-1-ylmethyl)piperidine(SALTDATA: 2HCl)

1.2 Other means of identification

Product number -
Other names -

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:90748-03-1 SDS

90748-03-1Downstream Products

90748-03-1Relevant academic research and scientific papers

PYRROLOPYRIMIDINE DERIVATIVES AS JAK3 INHIBITORS

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, (2008/12/04)

Pyrrolopyrimidine derivatives of formula (I), wherein the meanings for the various substituents are as disclosed in the description. These compounds are useful as JAK3 kinase inhibitors.

Farnesyl protein transferase inhibitors

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, (2008/06/13)

Disclosed are compounds of the formula: wherein R8represents a cyclic moiety to which is bound an imodazolylalkyl group; R9represents a carbamate, urea, amide or sulfonamide group; and the remaining substituents are as defined herein. Also disclosed is a method of treating cancer and a method of inhibiting farnesyl protein transferase using the disclosed compounds.

Penicillanic acid derivatives

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, (2008/06/13)

6-Amidinopenicillanic acid derivatives wherein one of the nitrogen atoms of the amidino group is part of a heterocyclic ring having on a side chain an unsubstituted heterocyclic ring containing 2 to 3 nitrogen atoms, and being useful as an antibiotic.

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