1. Home
  2. Benzoic acid, 2-hydroxy-, 4-nitrophenyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, 2-hydroxy-, 4-nitrophenyl ester

O=C(c1ccccc1O)Oc1ccc(cc1)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzoic acid, 2-hydroxy-, 4-nitrophenyl ester
CAS Number: 17374-48-0
Product Number: AG001Z5P(AGN-PC-0JT70M)
Synonyms:
MDL No:
Molecular Formula: C13H9NO5
Molecular Weight: 259.2143

Identification/Properties

Properties
MP:
148°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
259.217g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
259.048g/mol
Monoisotopic Mass:
259.048g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
332
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Nitrophenyl 2-hydroxybenzoate, also known as $name$, is a versatile compound widely utilized in organic chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable tool in the development of complex organic molecules with diverse functionalities. In chemical synthesis, $name$ can be employed as a key intermediate in the production of esters, ethers, and amides, playing a crucial role in the construction of new carbon-carbon and carbon-heteroatom bonds. Additionally, its presence in certain reactions can impart specific properties to the final products, such as enhanced stability, solubility, or bioactivity. Overall, the strategic use of 4-Nitrophenyl 2-hydroxybenzoate enables chemists to access novel compounds with tailored structures and properties for a wide range of applications in the fields of medicine, agriculture, and materials science.