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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)-

Cyclopentaneacetic acid, 3-oxo-2-pentyl-

CCCCCC1C(CCC1=O)CC(=O)O Request for Quotation
Chemical Name: Cyclopentaneacetic acid, 3-oxo-2-pentyl-
CAS Number: 3572-64-3
Product Number: AG00C9X0(AGN-PC-00S9S0)
Synonyms:
MDL No:
Molecular Formula: C12H20O3
Molecular Weight: 212.2854

Identification/Properties

Properties
BP:
361.9°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Computed Properties
Molecular Weight:
212.289g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
212.141g/mol
Monoisotopic Mass:
212.141g/mol
Topological Polar Surface Area:
54.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
235
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


2-(2-Butyl-4-oxocyclopentyl)acetic acid, also known as $name$, is a key intermediate in chemical synthesis with versatile applications. This compound plays a crucial role in organic chemistry as a building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its unique structure and reactivity, $name$ serves as a valuable starting material for the preparation of derivatives with desired properties.In chemical synthesis, $name$ can participate in a range of reactions such as esterification, amidation, and decarboxylation, leading to the formation of novel compounds with different functional groups and substitutions. Its cyclopentyl ring provides a rigid scaffold that can be modified to introduce specific stereochemistry and enhance molecular interactions in target molecules. Moreover, the butyl and acetic acid functionalities in $name$ offer synthetic flexibility, allowing for the introduction of diverse substituents to tailor the properties of the final product.The use of 2-(2-Butyl-4-oxocyclopentyl)acetic acid in chemical synthesis enables chemists to access structurally complex molecules efficiently and opens up opportunities for the development of new materials and active compounds with potential applications in various industries.