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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)-

Pentadecane, 5-methyl-

CCCCCCCCCCC(CCCC)C Request for Quotation
Chemical Name: Pentadecane, 5-methyl-
CAS Number: 25117-33-3
Product Number: AG0037IL(AGN-PC-0JKMRR)
Synonyms:
MDL No:
Molecular Formula: C16H34
Molecular Weight: 226.4412

Identification/Properties

Properties
MP:
-3.71°C (estimate)
BP:
277.27°C (estimate)
Storage:
Room Temperature;
Form:
Liquid
Refractive Index:
1.4224 (estimate)
Computed Properties
Molecular Weight:
226.448g/mol
XLogP3:
8.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
12
Exact Mass:
226.266g/mol
Monoisotopic Mass:
226.266g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
117
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


Pentadecane, 5-methyl- is a versatile chemical compound widely used in chemical synthesis for its unique properties and applications. As a linear hydrocarbon with a 15-carbon chain and a methyl group positioned at the 5th carbon, this compound plays a crucial role in various reactions and processes.One key application of Pentadecane, 5-methyl- in chemical synthesis is as a building block for the production of specialty chemicals and pharmaceuticals. Its long hydrocarbon chain provides a stable backbone for the synthesis of complex molecules, while the methyl group offers additional reactivity and functionality, allowing for the creation of diverse chemical structures.Furthermore, Pentadecane, 5-methyl- can serve as a solvent or diluent in chemical reactions, helping to control reaction conditions and improve product yield. Its nonpolar nature makes it a suitable medium for carrying out organic transformations, especially in reactions that require a hydrophobic environment.In addition, Pentadecane, 5-methyl- can act as a precursor in the synthesis of surfactants, lubricants, and other specialty chemicals. By incorporating this compound into the chemical structure of these products, manufacturers can enhance their performance, stability, and overall quality.Overall, Pentadecane, 5-methyl- is a valuable tool in chemical synthesis, offering a range of applications that contribute to the development of new materials, pharmaceuticals, and industrial compounds. Its unique structure and reactivity make it an essential ingredient in the toolkit of synthetic chemists seeking to create novel molecules and products.