What is the 2-BENZYLPIPERIDINE?

2-BENZYLPIPERIDINE is , while it's Molecular Formula is C12H17N. Used in Scientific Research: 2-Benzylpiperidine is used as a research compound in the field of organic chemistry for [application reason]. It is not widely used in commerce or industry, but its unique structure and properties make it valuable for studying chemical reactions and interactions. Used in Organic Chemistry: 2-Benzylpiperidine is used as a building block or intermediate in the synthesis of more complex organic molecules for [application reason]. Its presence in the benzylpiperidine class allows for the exploration of various chemical modifications and the development of new compounds with potential applications in different areas.

What is the CAS number for 2-BENZYLPIPERIDINE?

The CAS number of 2-BENZYLPIPERIDINE is 32838-55-4.

What is 2-BENZYLPIPERIDINE (32838-55-4) used for?

2-Benzylpiperidine is a chemical compound that belongs to the class of organic compounds known as benzylpiperidines. These are aromatic compounds containing a piperidine ring that is substituted by a benzyl group. It has a molecular formula of C12H17N and is typically synthesized with a purity above 98%. 2-BENZYLPIPERIDINE is characterized by an ammonia-like aroma and, as a base, forms salts upon reaction with acids.InChI:InChI=1/C12H17N.ClH/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12;/h1-3,6-7,12-13H,4-5,8-10H2;1H

What is the 2-BENZYLPIPERIDINE?

2-BENZYLPIPERIDINE is , while it's Molecular Formula is C12H17N. Used in Scientific Research: 2-Benzylpiperidine is used as a research compound in the field of organic chemistry for [application reason]. It is not widely used in commerce or industry, but its unique structure and properties make it valuable for studying chemical reactions and interactions. Used in Organic Chemistry: 2-Benzylpiperidine is used as a building block or intermediate in the synthesis of more complex organic molecules for [application reason]. Its presence in the benzylpiperidine class allows for the exploration of various chemical modifications and the development of new compounds with potential applications in different areas.

What is the CAS number for 2-BENZYLPIPERIDINE?

The CAS number of 2-BENZYLPIPERIDINE is 32838-55-4.

What is 2-BENZYLPIPERIDINE (32838-55-4) used for?

2-Benzylpiperidine is a chemical compound that belongs to the class of organic compounds known as benzylpiperidines. These are aromatic compounds containing a piperidine ring that is substituted by a benzyl group. It has a molecular formula of C12H17N and is typically synthesized with a purity above 98%. 2-BENZYLPIPERIDINE is characterized by an ammonia-like aroma and, as a base, forms salts upon reaction with acids.InChI:InChI=1/C12H17N.ClH/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12;/h1-3,6-7,12-13H,4-5,8-10H2;1H

Current location：Home > Products > 2-BENZYLPIPERIDINE

2-BENZYLPIPERIDINE

Name 2-BENZYLPIPERIDINE
CAS 32838-55-4
Purity 99%

Inquiry

Product Details

Buy reliable Quality 2-BENZYLPIPERIDINE 32838-55-4 raw material with Honest Price

Molecular Formula: C12H17N
Molecular Weight: 175.274
Vapor Pressure: 0.000698mmHg at 25°C
Melting Point: 32°C
Refractive Index: 1.5227 (estimate)
Boiling Point: 267.5 °C at 760 mmHg
PKA: 10.55±0.10(Predicted)
Flash Point: 116.129 °C
PSA： 12.03000
Density: 0.969 g/cm³
LogP: 2.70000

2-BENZYLPIPERIDINE(Cas 32838-55-4) Usage

General Description

2-Benzylpiperidine is a chemical compound that belongs to the class of organic compounds known as benzylpiperidines. These are aromatic compounds containing a piperidine ring that is substituted by a benzyl group. Its molecular formula is C12H17N, and its purity is typically above 98% when synthesized. It has an aroma that has been described as ammonia-like, and as a base, this compound forms salts upon reaction with acids. 2-Benzylpiperidine is not widely used in commerce or industry. However, it has been utilized in scientific research, particularly in the field of organic chemistry.

InChI:InChI=1/C12H17N.ClH/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12;/h1-3,6-7,12-13H,4-5,8-10H2;1H

32838-55-4 Relevant articles

-

Faraj et al.

, p. 20,24 (1976)

Hydrogenation of 2-benzylpyridine over alumina-supported Ru catalysts: Use of Ru3(CO)12 as a Ru precursor

Kim, Tae Wan,Oh, Jinho,Suh, Young-Woong

, p. 183 - 190 (2017)

Although Ru3(CO)12 becomes a popular pre...

Synthesis and pharmacology of site-specific cocaine abuse treatment agents: Restricted rotation analogues of methylphenidate

Kim, Deog-Il,Deutsch, Howard M.,Ye, Xiaocong,Schweri, Margaret M.

, p. 2718 - 2731 (2007)

A series of threo-1-aza-3 or 4-substitut...

PRODUCTION METHOD OF CYCLIC COMPOUND

-

Paragraph 0057; 0059; 0062-0064, (2021/05/05)

PROBLEM TO BE SOLVED: To provide an indu...

Construction of azacycles by intramolecular amination of organoboronates and organobis(boronates)

Xu, Peilin,Zhang, Mingkai,Ingoglia, Bryan,Allais, Christophe,Dechert-Schmitt, Anne-Marie R.,Singer, Robert A.,Morken, James P.

, p. 3379 - 3383 (2021/05/10)

Intramolecular amination of organoborona...

Synthetic Cathinone Analogues Structurally Related to the Central Stimulant Methylphenidate as Dopamine Reuptake Inhibitors

Yadav-Samudrala, Barkha J.,Eltit, Jose M.,Glennon, Richard A.

, p. 4043 - 4050 (2019/09/07)

Synthetic cathinones are, primarily, sti...

Structure Kinetics Relationships and Molecular Dynamics Show Crucial Role for Heterocycle Leaving Group in Irreversible Diacylglycerol Lipase Inhibitors

Janssen, Antonius P.A.,Van Hengst, Jacob M.A.,Béquignon, Olivier J.M.,Deng, Hui,Van Westen, Gerard J.P.,Van Der Stelt, Mario

, p. 7910 - 7922 (2019/10/11)

Drug discovery programs of covalent irre...

32838-55-4 Process route

: 91-02-1
phenyl(pyridin-2-yl)methanone

: 32838-55-4
2-benzylpiperidine

Conditions

Conditions	Yield
With palladium on activated charcoal; hydrogen; acetic acid; at 20 ℃; for 8h; under 760.051 Torr;	100%
Multi-step reaction with 2 steps 1: acetic acid; platinum on carbon; hydrogen / 6 h / 1551.49 - 2068.65 Torr 2: acetic acid; perchloric acid; platinum on carbon; hydrogen / 72 h / 50 - 55 Torr With perchloric acid; platinum on carbon; hydrogen; acetic acid;

: 89656-42-8
[1-(2-Benzyl-piperidin-1-yl)-meth-(E)-ylidene]-tert-butyl-amine

: 32838-55-4
2-benzylpiperidine

Conditions

Conditions	Yield
With potassium hydroxide; In methanol; water; at 60 ℃; for 12h;	87%

32838-55-4 Upstream products

101-82-6
2-Benzylpyridine
89656-42-8
[1-(2-Benzyl-piperidin-1-yl)-meth-(E)-ylidene]-tert-butyl-amine
95018-41-0
2-benzyl-3,4,5,6-tetrahydropyridine
89656-42-8
[1-(2-Benzyl-piperidin-1-yl)-meth-(E)-ylidene]-tert-butyl-amine

32838-55-4 Downstream products

31414-56-9
N-Methyl-2-(phenylmethyl)piperidine
93683-90-0
5'-Amino-2-benzyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-6'-carbonitrile
93684-05-0
6-(2-Benzyl-piperidin-1-yl)-pyrido[3,2-d]pyrimidine-2,4-diamine
228877-86-9
N-chloroacetyl-2-benzylpiperidine

Home

About Us

Products

Pharmaceutical

Organic Chemicals

Agrochemicals

Others

News

Contact Us