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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)-

Butanoic acid, 3-methyl-, pentyl ester

CCCCCOC(=O)CC(C)C Request for Quotation
Chemical Name: Butanoic acid, 3-methyl-, pentyl ester
CAS Number: 25415-62-7
Product Number: AG01CKLT(AGN-PC-0JM1LY)
Synonyms:
MDL No:
Molecular Formula: C10H20O2
Molecular Weight: 172.2646

Identification/Properties

Computed Properties
Molecular Weight:
172.268g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
7
Exact Mass:
172.146g/mol
Monoisotopic Mass:
172.146g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
119
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


Pentyl isopentanoate is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. As an ester, it serves as an excellent solvent in organic reactions, particularly in Fischer esterification and transesterification processes. Its high solvency power makes it an ideal medium for dissolving a wide range of organic compounds, enabling efficient mixing and reaction to occur.In addition to its role as a solvent, Pentyl isopentanoate also functions as a valuable reagent in the production of various aromatic and aliphatic compounds. Its ester group can undergo hydrolysis reactions under controlled conditions to yield carboxylic acids and alcohols, which can then be further transformed into diverse chemical products. Furthermore, its ester linkage can participate in nucleophilic substitution reactions, allowing for the synthesis of more complex molecules.Overall, Pentyl isopentanoate plays a crucial role in chemical synthesis by enabling the formation of new chemical bonds and facilitating the creation of intricate organic structures. Its versatility and reactivity make it an indispensable component in the toolkit of synthetic chemists seeking to develop novel compounds and materials for a wide range of applications.