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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, 2,6-diethyl-

CCc1cccc(n1)CC Request for Quotation
Chemical Name: Pyridine, 2,6-diethyl-
CAS Number: 935-28-4
Product Number: AG00GUHX(AGN-PC-0JMP29)
Synonyms:
MDL No:
Molecular Formula: C9H13N
Molecular Weight: 135.2062

Identification/Properties

Computed Properties
Molecular Weight:
135.21g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
135.105g/mol
Monoisotopic Mass:
135.105g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
80.7
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Diethylpyridine is a versatile organic compound widely utilized in chemical synthesis. Due to its unique molecular structure, this compound serves as a vital building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, 2,6-Diethylpyridine plays a crucial role as a ligand in catalytic reactions, facilitating the formation of complex organic molecules with high efficiency and selectivity. Its application in the development of novel materials and the preparation of functionalized intermediates underscores its significance in modern chemical research. Additionally, 2,6-Diethylpyridine is employed as a key intermediate in the synthesis of pyridine-based derivatives, making it a valuable asset in the production of diverse chemical compounds with broad industrial applications.