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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)-

Pentanoic acid, 4-bromo-

CC(CCC(=O)O)Br Request for Quotation
Chemical Name: Pentanoic acid, 4-bromo-
CAS Number: 1450-80-2
Product Number: AG01A3UF(AGN-PC-00PPJO)
Synonyms:
MDL No:
Molecular Formula: C5H9BrO2
Molecular Weight: 181.0278

Identification/Properties

Computed Properties
Molecular Weight:
181.029g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
179.979g/mol
Monoisotopic Mass:
179.979g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
82.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


4-Bromopentanoic acid, also known as 4-Bromovaleric acid, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, 4-Bromopentanoic acid serves as a valuable building block for the synthesis of various organic compounds, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals.One of the key applications of 4-Bromopentanoic acid is as a precursor in the synthesis of pharmaceutical intermediates. It can be utilized in the preparation of active pharmaceutical ingredients (APIs) and drug molecules through diverse chemical transformations such as nucleophilic substitution reactions, esterifications, and amidations. The presence of the bromine substituent enhances the reactivity of the molecule, allowing for selective functionalization at the bromine position to introduce specific functional groups required for target molecules.In addition to its role in pharmaceutical chemistry, 4-Bromopentanoic acid finds application in the synthesis of agrochemicals. By serving as a starting material for the construction of complex structures, this compound enables the efficient production of herbicides, insecticides, and fungicides that play a crucial role in modern agriculture. The ability to modify the molecular structure of 4-Bromopentanoic acid through various synthetic routes makes it a valuable tool for designing novel agrochemical compounds with improved efficacy and environmental safety profiles.Furthermore, 4-Bromopentanoic acid is employed in the synthesis of specialty chemicals and fine chemicals for various industrial applications. Its versatile reactivity allows for the incorporation of specific functional groups and modifications, making it a valuable intermediate in the custom synthesis of organic molecules tailored to specific industrial requirements. From polymer additives to flavors and fragrances, 4-Bromopentanoic acid contributes to the development of a wide range of high-value chemical products essential for diverse industries.Overall, the strategic use of 4-Bromopentanoic acid in chemical synthesis highlights its significance as a key building block for creating complex organic molecules with tailored properties for pharmaceutical, agrochemical, and industrial applications. Its versatility and reactivity make it a valuable tool for organic chemists seeking to develop innovative chemical solutions for various industries.