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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, 5-chloro-

ClCCCCC(=O)O Request for Quotation
Chemical Name: Pentanoic acid, 5-chloro-
CAS Number: 1119-46-6
Product Number: AG00349E(AGN-PC-0JKBMU)
Synonyms:
MDL No:
Molecular Formula: C5H9ClO2
Molecular Weight: 136.5768

Identification/Properties

Properties
MP:
18 °C
BP:
230.0°C
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.454(lit.)
Computed Properties
Molecular Weight:
136.575g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
136.029g/mol
Monoisotopic Mass:
136.029g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
72.8
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


5-Chlorovaleric Acid, also known as pentanoic acid, is a highly versatile compound frequently employed in chemical synthesis processes. Its unique chemical structure and reactivity make it a valuable building block for the creation of various organic compounds and materials. In chemical synthesis, 5-Chlorovaleric Acid serves as a crucial intermediate for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its presence enables the formation of complex molecular structures through reactions such as esterification, amidation, and hydrogenation. Additionally, 5-Chlorovaleric Acid plays a key role in the production of specialty polymers and materials used in the manufacturing of adhesives, coatings, and surfactants. Its ability to participate in a wide range of chemical transformations makes it an indispensable component in the toolbox of synthetic chemists seeking to create novel compounds with tailored properties and functions.