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1-(Piperidin-3-yl)ethanol is an organic compound with the molecular formula C7H15NO. It is a colorless liquid at room temperature and is soluble in water. This chemical is a derivative of ethanol, where one of the hydrogen atoms on the carbon chain is replaced by a piperidin-3-yl group, which is a cyclic amine containing a six-membered nitrogen-containing ring. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure that can be further functionalized. The compound is also known for its potential applications in the development of new drugs, particularly in the area of central nervous system medications, where its ability to interact with specific receptors can be exploited.

5434-88-8

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5434-88-8 Usage

Chemical class

Alcohols

Usage

Building block in organic synthesis

Industry application

Pharmaceutical industry

Synthesis purpose

Creation of various drugs and pharmaceutical intermediates

Structural feature

Piperidine ring with a hydroxyethyl group attached to the nitrogen atom

Versatility

Allows for the synthesis of a wide range of pharmaceutical compounds

Additional use

Chiral resolving agent in the separation of racemic mixtures

Check Digit Verification of cas no

The CAS Registry Mumber 5434-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5434-88:
(6*5)+(5*4)+(4*3)+(3*4)+(2*8)+(1*8)=98
98 % 10 = 8
So 5434-88-8 is a valid CAS Registry Number.

5434-88-8SDS

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 1-piperidin-3-ylethanol

1.2 Other means of identification

Product number -
Other names methyl-3-piperidinylmethanol

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:5434-88-8 SDS

5434-88-8Relevant academic research and scientific papers

ISOXAZOLE DERIVATIVES AS MODULATORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1

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Page/Page column 22, (2009/08/16)

The present invention relates to novel isoxazole compounds of formula (I), and pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides thereof, which are modulators of 11?-hydroxysteroid dehydroge

Pleuromutilin derivatives as antimicrobials

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, (2008/06/13)

The present invention relates to pleuromutilin derivatives, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medical therapy, particularly antibacterial therapy.

Antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones

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, (2008/06/13)

This invention relates to compounds of Formula I STR1 which are useful in association with a pharmaceutical carrier as antiatherosclerotic agents. In addition, various compounds of Formula I are useful inhibitors of cell proliferation.

Antiatherosclerotic and antithrombotic 2-amino-6-phenyl-4H-pyran-4-ones

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, (2008/06/13)

This invention relates to compounds of Formula I STR1 which are useful as antiatherosclerotic agents and inhibitors of cell proliferation for the treatment of proliferative diseases. In addition, various compounds of Formula I are useful inhibitors of platelet aggregation.

Treatment of atherosclerosis with khellin-related furochromones

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, (2008/06/13)

The present specification relates to the antiatherosclerotic use of khellin and related furochromones, and further provides novel antiatherogenic furochromones.

Antiatherosclerotic furochromones

-

, (2008/06/13)

The present specification relates to the antiatherosclerotic use of khellin and related furochromones, and further provides novel antiatherogenic furochromones.

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