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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)-

Benzoic acid, 4-amino-, monopotassium salt

[O-]C(=O)c1ccc(cc1)N.[K+] Request for Quotation
Chemical Name: Benzoic acid, 4-amino-, monopotassium salt
CAS Number: 138-84-1
Product Number: AG0017SU(AGN-PC-0PNEE9)
Synonyms:
MDL No:
Molecular Formula: C7H6KNO2
Molecular Weight: 175.2263

Identification/Properties

Properties
BP:
339.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
175.228g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
175.004g/mol
Monoisotopic Mass:
175.004g/mol
Topological Polar Surface Area:
66.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
132
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Potassium 4-aminobenzoate, also known as Potassium p-aminobenzoate, is a versatile chemical compound widely utilized in various chemical synthesis processes. As a key intermediate in organic chemistry, Potassium 4-aminobenzoate plays a critical role in the production of pharmaceuticals, dyes, and polymers.In chemical synthesis, Potassium 4-aminobenzoate serves as a crucial building block for the synthesis of diverse compounds due to its unique structural properties. It can be used in the preparation of various pharmaceuticals, including anti-inflammatory drugs, local anesthetics, and antibacterial agents. Additionally, this compound is instrumental in the synthesis of dyes, enabling the creation of vibrant and stable colorants for textile and cosmetic applications.Furthermore, Potassium 4-aminobenzoate finds utility in polymer chemistry, where it functions as a monomer for producing specialty polymers with specific properties. By incorporating Potassium 4-aminobenzoate into polymerization reactions, researchers can tailor the physical and chemical characteristics of the resulting polymers to meet desired specifications.Overall, the versatile applications of Potassium 4-aminobenzoate make it an indispensable compound in chemical synthesis, offering a wide range of possibilities for the creation of valuable products across various industries.