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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyridine, pentyl-

CCCCCc1ccccn1 Request for Quotation
Chemical Name: Pyridine, pentyl-
CAS Number: 2294-76-0
Product Number: AG002LLG(AGN-PC-0JKD3L)
Synonyms:
MDL No:
Molecular Formula: C10H15N
Molecular Weight: 149.2328

Identification/Properties

Properties
BP:
210.4°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.488(lit.)
Computed Properties
Molecular Weight:
149.237g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
149.12g/mol
Monoisotopic Mass:
149.12g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
90.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H227-H315-H319-H335
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Pentylpyridine is a versatile compound commonly used in chemical synthesis. With its unique structure and properties, this compound plays a crucial role in various reactions and processes within the field of organic chemistry. One of the key applications of 2-Pentylpyridine in chemical synthesis is as a reagent for the preparation of heterocyclic compounds. Due to its aromatic nature and functional group positioning, 2-Pentylpyridine can serve as a building block in the construction of complex molecular structures, particularly in the synthesis of pharmaceuticals, agrochemicals, and materials science. The presence of the pyridine ring in 2-Pentylpyridine also allows for facile functionalization and derivatization, making it a valuable tool for modifying and fine-tuning the properties of target molecules. Additionally, 2-Pentylpyridine can act as a ligand in catalytic processes, enabling the efficient formation of carbon-carbon and carbon-nitrogen bonds in various chemical transformations. Its broad applicability and versatility make 2-Pentylpyridine a valuable resource in the arsenal of synthetic chemists seeking to access novel and functionalized compounds for diverse applications.