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66898-97-3

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66898-97-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The compound is derived from piperidine, a heterocyclic amine, with an additional trifluoromethylbenzyl group attached, which influences its properties and potential applications.

Explanation

These functional groups contribute to the compound's reactivity, stability, and potential interactions with other molecules.

Explanation

Due to its unique structure, 1-[3-(trifluoromethyl)benzyl]piperidin-4-amine can be used as a starting material for the synthesis of more complex molecules.

Explanation

The compound is sometimes used in research and pharmaceutical development, particularly for creating compounds that target the central nervous system.

Explanation

The compound's specific properties and potential applications depend on additional research and testing to understand its interactions with biological systems and other molecules.

Explanation

The solubility of the compound in various solvents is not provided and would require experimental data for determination.

Explanation

The stability of the compound under different conditions (e.g., temperature, pH, light exposure) is not provided and would require experimental data for determination.

Explanation

The reactivity of the compound with other chemicals or under specific conditions is not provided and would require experimental data for determination.

Chemical structure

Piperidine derivative with a trifluoromethylbenzyl group attached to the piperidine ring

Functional groups

Piperidine, trifluoromethyl, and amine groups

Application

Building block for creating other chemical compounds

Target

Central nervous system

Further research and testing

Required for specific properties and potential uses

Solubility

Unknown without experimental data

Stability

Unknown without experimental data

Reactivity

Unknown without experimental data

Check Digit Verification of cas no

The CAS Registry Mumber 66898-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,9 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66898-97:
(7*6)+(6*6)+(5*8)+(4*9)+(3*8)+(2*9)+(1*7)=203
203 % 10 = 3
So 66898-97-3 is a valid CAS Registry Number.

66898-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[[3-(trifluoromethyl)phenyl]methyl]piperidin-4-amine

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:66898-97-3 SDS

66898-97-3Relevant articles and documents

Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation

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, (2015/09/28)

Heterocyclic aromatic amides having a hydroxy group adjacent to the amide functionality are useful as antifungal agents, particularly for plants.

6,9-DISUBSTITUTED 2- TRANS-(4- AMINOCYCLOHEXYL) AMINO]PURINES

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Page/Page column 140, (2008/06/13)

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The design and synthesis of purine inhibitors of CDK2. III

Shum,Peet,Weintraub,Le,Zhao,Barbone,Cashman,Tsay,Dwyer,Loos,Powers,Kropp,Wright,Bitonti,Dumont,Borcherding

, p. 1067 - 1078 (2007/10/03)

Cyclin-dependent kinases (CDKs) belong to a class of enzymes that control the ability of a cell to enter into and proceed through the cell division cycle. Using purine as a scaffold, we have synthesized a number of nanomolar inhibitors of CDK-2/cyclin E. In this report, the synthesis of a series of piperidine-substituted purine analogs will be presented, as well as some of their in vitro and in vivo biological effects.

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