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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)-

Benzonitrile, 3-hydroxy-5-methyl-

N#Cc1cc(C)cc(c1)O Request for Quotation
Chemical Name: Benzonitrile, 3-hydroxy-5-methyl-
CAS Number: 95658-81-4
Product Number: AG005ZD7(AGN-PC-03I6CW)
Synonyms:
MDL No:
Molecular Formula: C8H7NO
Molecular Weight: 133.1473

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
133.15g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
133.053g/mol
Monoisotopic Mass:
133.053g/mol
Topological Polar Surface Area:
44A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
158
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-methylbenzonitrile, also known as 3-Hydroxy-5-methylbenzene-1-carbonitrile, plays a crucial role in chemical synthesis as a versatile building block for various organic compounds. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Its hydroxyl and nitrile functional groups offer reactivity and enable its involvement in various synthetic pathways. 3-Hydroxy-5-methylbenzonitrile can undergo a range of chemical reactions including nucleophilic substitution, oxidation, and condensation reactions, making it a valuable starting material for creating complex molecular structures.In pharmaceutical synthesis, this compound can be utilized for the construction of biologically active molecules such as antiviral agents, enzyme inhibitors, and aromatic heterocycles. Its presence in the agrochemical industry contributes to the production of pesticides, herbicides, and fungicides that play a crucial role in crop protection.Overall, the versatility and reactivity of 3-Hydroxy-5-methylbenzonitrile make it an important component in the realm of chemical synthesis, enabling the creation of diverse compounds with significant applications in various industries.