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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)-

3-hydroxy-5-nitrobenzonitrile

N#Cc1cc(O)cc(c1)[N+](=O)[O-] Request for Quotation
Chemical Name: 3-hydroxy-5-nitrobenzonitrile
CAS Number: 929000-02-2
Product Number: AG006KTM(AGN-PC-058A03)
Synonyms:
MDL No: MFCD09258662
Molecular Formula: C7H4N2O3
Molecular Weight: 164.1183

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
164.12g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
164.022g/mol
Monoisotopic Mass:
164.022g/mol
Topological Polar Surface Area:
89.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
227
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


3-Hydroxy-5-nitrobenzonitrile is a versatile compound that finds widespread application in chemical synthesis. As a key intermediate in organic chemistry, this compound serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structural properties make it particularly useful in the development of advanced materials and specialized chemical processes.One of the primary applications of 3-Hydroxy-5-nitrobenzonitrile is its involvement in the synthesis of biologically active compounds. By serving as a precursor in the production of pharmaceutical ingredients, this compound plays a vital role in the pharmaceutical industry. Researchers and chemists utilize its distinctive reactivity to introduce specific functional groups and achieve desired molecular structures, enabling the synthesis of novel drugs with potential therapeutic benefits.Furthermore, 3-Hydroxy-5-nitrobenzonitrile is instrumental in the production of agrochemicals. Its incorporation into pesticide formulations and herbicidal compounds allows for the development of potent plant protection products. By engaging in chemical reactions that modify its chemical structure, this compound contributes to the enhancement of agricultural practices and the protection of crops from pests and diseases.In addition to its applications in pharmaceuticals and agrochemicals, 3-Hydroxy-5-nitrobenzonitrile is also utilized in the synthesis of fine chemicals. Its role in creating specialty chemicals, dyes, and advanced materials underscores its importance in various industrial sectors. Chemists employ this compound to design and manufacture specialized compounds that exhibit unique properties and functionalities, catering to diverse industrial and commercial needs.Overall, 3-Hydroxy-5-nitrobenzonitrile serves as a valuable component in chemical synthesis, offering a wide range of applications in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its versatility and reactivity make it a sought-after intermediate in organic chemistry, driving innovation and progress in the field of chemical research and production.