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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)-

Benzenebutanoic acid, 3-amino-, hydrochloride

OC(=O)CCCc1cccc(c1)N.Cl Request for Quotation
Chemical Name: Benzenebutanoic acid, 3-amino-, hydrochloride
CAS Number: 91843-18-4
Product Number: AG00GXYH(AGN-PC-00EOXL)
Synonyms:
MDL No:
Molecular Formula: C10H14ClNO2
Molecular Weight: 215.6767

Identification/Properties

Properties
MP:
140-152 °C
Storage:
2-8℃;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
215.677g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
215.071g/mol
Monoisotopic Mass:
215.071g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
170
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3-Aminophenyl)butanoic acid hydrochloride is commonly used in chemical synthesis as a versatile building block for pharmaceuticals and organic compounds. Its unique structure and reactivity make it a valuable intermediate in the synthesis of various drugs, including analgesics, anti-inflammatory agents, and cardiovascular medications. With its functional groups offering key opportunities for derivatization, this compound plays a crucial role in creating novel molecules with targeted biological activities. Additionally, its hydrochloride form enhances solubility and stability in aqueous solutions, facilitating its use in a wide range of synthetic processes.