2-(3-PENTYL)PYRIDINE

  • Name: 2-(3-PENTYL)PYRIDINE
  • CAS: 7399-50-0
  • Purity: 99%
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Details

Top Quality 2-(3-PENTYL)PYRIDINE 7399-50-0 Hot Sell In Stock

  • Molecular Formula: C10H15 N
  • Molecular Weight: 149.236
  • Vapor Pressure: 0.589mmHg at 25°C 
  • Melting Point: 125.5°C (estimate) 
  • Refractive Index: 1.4860 to 1.4880 
  • Boiling Point: 195.4°Cat760mmHg 
  • PKA: 5.65±0.19(Predicted) 
  • Flash Point: 51.3°C 
  • PSA： 12.89000 
  • Density: 0.9g/cm3 
  • LogP: 2.98520 

2-(3-PENTYL)PYRIDINE(Cas 7399-50-0) Usage

General Description

2-(3-Pentyl)pyridine is a chemical compound that belongs to the class of organic compounds known as aryl-alcohols. It is primarily characterized by its structure that contains a pentyl group (a five-carbon chain) attached to the third position of a pyridine ring. Pyridine is a basic heterocyclic organic compound structurally related to benzene, and like benzene it is a colorless liquid that is highly flammable. 2-(3-PENTYL)PYRIDINE is not commonly found in a typical human biochemistry, but has important applications in various industries such as in pharmaceuticals, agrochemicals, food, and others due to its reactivity and structure. Specific properties such as boiling point, melting point or toxicity of 2-(3-Pentyl)pyridine may vary depending on its form and purity.

InChI:InChI=1/C10H15N/c1-3-9(4-2)10-7-5-6-8-11-10/h5-9H,3-4H2,1-2H3

7399-50-0 Relevant articles

Barbier–Negishi Coupling of Secondary Alkyl Bromides with Aryl and Alkenyl Triflates and Nonaflates

Zhang, Ke-Feng,Christoffel, Fadri,Baudoin, Olivier

supporting information, p. 1982 - 1986 (2018/02/06)

A mild and practical Barbier–Negishi cou...

Terminal-Selective Functionalization of Alkyl Chains by Regioconvergent Cross-Coupling

Dupuy, Stéphanie,Zhang, Ke-Feng,Goutierre, Anne-Sophie,Baudoin, Olivier

supporting information, p. 14793 - 14797 (2016/11/23)

Hydrocarbons are still the most importan...

TRANSITION METAL-CATALYZED ALKYLATION OF C-H BONDS WITH ORGANOBORON REAGENTS

-

, (2008/06/13)

One aspect of the present invention rela...

Palladium-catalyzed alkylation of sp2 and sp3 C-H bonds with methylboroxine and alkylboronic acids: Two distinct C-H activation pathways

Chen, Xiao,Goodhue, Charles E.,Yu, Jin-Quan

, p. 12634 - 12635 (2008/02/05)

Palladium-catalyzed alkylations of sp2 a...

7399-50-0 Process route

α-picoline
109-06-8

α-picoline

ethene
74-85-1

ethene

2-propylpyridine
622-39-9

2-propylpyridine

2-(1-ethylpropyl)-pyridine
7399-50-0

2-(1-ethylpropyl)-pyridine

Conditions
Conditions Yield
With sodium; at 160 ℃; under 22065.2 Torr;
α-picoline
109-06-8

α-picoline

2-propylpyridine
622-39-9

2-propylpyridine

2-(1-ethylpropyl)-pyridine
7399-50-0

2-(1-ethylpropyl)-pyridine

Conditions
Conditions Yield
With hexane; sodium amide; at 100 ℃; anschliessend Behandeln mit Aethylen bei 160-170grad/25-35 at;
With 2-picolyl-sodium; hexane; at 100 ℃; anschliessend Behandeln mit Aethylen bei 160-170grad/25-35 at;

7399-50-0 Upstream products

  • 109-06-8
    109-06-8

    α-picoline

  • 74-85-1
    74-85-1

    ethene

  • 622-39-9
    622-39-9

    2-propylpyridine

  • 644-98-4
    644-98-4

    2-isopropylpyridine

7399-50-0 Downstream products

  • 103906-20-3
    103906-20-3

    2-(1-ethylpropyl)piperidine

  • 1079883-81-0
    1079883-81-0

    2-(3,5-dimethylphenyl)-6-(1-ethylpropyl)-pyridine

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