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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-(4-cyanophenoxy)-

N#Cc1ccc(cc1)Oc1ccc(cc1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 4-(4-cyanophenoxy)-
CAS Number: 50793-29-8
Product Number: AG00DLUM(AGN-PC-0KD2OQ)
Synonyms:
MDL No:
Molecular Formula: C14H9NO3
Molecular Weight: 239.2262

Identification/Properties

Computed Properties
Molecular Weight:
239.23g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
239.058g/mol
Monoisotopic Mass:
239.058g/mol
Topological Polar Surface Area:
70.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
330
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(4-Cyanophenoxy)benzoic acid, also known as CYA acid, plays a crucial role in chemical synthesis as a versatile building block for the creation of novel compounds and functional materials. This chemical is widely utilized in organic synthesis due to its unique chemical structure and reactivity.One key application of 4-(4-Cyanophenoxy)benzoic acid is in the production of pharmaceuticals and agrochemicals. Its functional groups enable the attachment of various substituents, allowing for the synthesis of complex molecules with specific biological activities. Researchers often use CYA acid as a starting material for the development of new drugs and crop protection agents.Additionally, this compound is commonly employed in the field of materials science. By manipulating the chemical structure of 4-(4-Cyanophenoxy)benzoic acid through reactions such as esterification or amidation, researchers can create polymers and materials with tailored properties. These materials find applications in areas such as coatings, adhesives, and electronic devices.Furthermore, 4-(4-Cyanophenoxy)benzoic acid serves as a valuable intermediate in the synthesis of dyes and pigments. Its aromatic structure makes it a suitable precursor for the preparation of colored compounds used in various industries, including textiles and cosmetics.Overall, the versatility of 4-(4-Cyanophenoxy)benzoic acid in chemical synthesis makes it a valuable tool for the development of a wide range of products across different sectors. Its ability to undergo diverse chemical transformations makes it an essential building block for the creation of innovative molecules with desired properties.