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24448-89-3

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24448-89-3 Usage

General Description

3-Piperidin-2-yl-propan-1-ol is a chemical compound that belongs to the class of organic compounds known as piperidines. It’s known for its role as a metabolite, a crucial mechanism involved in enzyme activations or deactivation, gene expression, and protein synthesis. It contains a piperidine ring, which is a saturated heterocycle made up of five methylene bridges (-CH2-) and one amine bridge (-NH-). The structure is based on the piperidine skeleton, which deviates with the attachment of a methylene group (-CH2-) on a piperidine nitrogen atom (-NH-). Due to its structural characteristics, it is likely to be involved in biological activities like molecular binding and signal transduction. However, information on its specific industrial or pharmaceutical applications is somewhat limited.

Check Digit Verification of cas no

The CAS Registry Mumber 24448-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,4 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24448-89:
(7*2)+(6*4)+(5*4)+(4*4)+(3*8)+(2*8)+(1*9)=123
123 % 10 = 3
So 24448-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO/c10-7-3-5-8-4-1-2-6-9-8/h8-10H,1-7H2

24448-89-3 Well-known Company Product Price

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  • Aldrich

  • (CBR01786)  3-Piperidin-2-ylpropan-1-ol  AldrichCPR

  • 24448-89-3

  • CBR01786-1G

  • 4,512.69CNY

  • Detail

24448-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Piperidin-2-ylpropan-1-ol

1.2 Other means of identification

Product number -
Other names 3-piperidin-2-ylpropan-1-ol

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:24448-89-3 SDS

24448-89-3Relevant articles and documents

PRODUCTION METHOD OF CYCLIC COMPOUND

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Paragraph 0057; 0060; 0062; 0065, (2021/05/05)

PROBLEM TO BE SOLVED: To provide an industrially simple production method of a cyclic compound. SOLUTION: A production method of a cyclic compound includes a step to obtain a reduced form (B) by reducing an unsaturated bond in a ring structure of an aromatic compound (A) by means of catalytic hydrogenation of the aromatic compound (A) or its salt using palladium carbon as a catalyst under a normal pressure, in which the aromatic compound (A) has one or more ring structures selected from a group consisting of a five membered-ring, a six membered-ring, and a condensed ring of the five membered-ring or the six membered-ring with another six membered-ring, a hetero atom can be included in the ring structure, and the aromatic compound (A) can have one or two side chains bonded to the ring structure and does not have any carbon-carbon triple bond in the side chain. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

METHOD FOR PRODUCING PIPERIDINE COMPOUND

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Paragraph 0057; 0058; 0060-0063, (2018/04/18)

PROBLEM TO BE SOLVED: To provide a method for producing a piperidine compound in an industrially convenient manner. SOLUTION: This invention relates to a method for producing a compound represented by general formula (I) or a salt thereof that includes the step of converting a pyridine compound having an alkynylene group in a side chain, by a contact hydrogenation reaction, into the compound represented by general formula (I) or a salt thereof (in the general formula (I), R1 is a hydrogen atom, a hydroxy group, or an optionally substituted alkyl group having carbon atoms of 1 or more and 20 or less). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

Chemokine receptor binding heterocyclic compounds with enhanced efficacy

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Page/Page column 26-27, (2010/02/03)

The invention relates to heterocyclic compounds consisting of a core nitrogen atom surrounded by three pendant groups, wherein two of the three pendant groups are preferably benzimidazolyl methyl and tetrahydroquinolyl, and the third pendant group contains N and optionally contains additional rings. The compounds bind to chemokine receptors, including CXCR4 and CCR5, and demonstrate protective effects against infection of target cells by a human immunodeficiency virus (HIV).

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