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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)-

Benzenemethanol, 4-(1H-1,2,4-triazol-1-yl)-

OCc1ccc(cc1)n1ncnc1 Request for Quotation
Chemical Name: Benzenemethanol, 4-(1H-1,2,4-triazol-1-yl)-
CAS Number: 143426-50-0
Product Number: AG003JXO(AGN-PC-0KKXKH)
Synonyms:
MDL No: MFCD02682061
Molecular Formula: C9H9N3O
Molecular Weight: 175.1873

Identification/Properties

Properties
MP:
124-126°C
BP:
383°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
175.191g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
175.075g/mol
Monoisotopic Mass:
175.075g/mol
Topological Polar Surface Area:
50.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
157
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-(1,2,4-Triazol-1-yl)benzyl alcohol, commonly known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, $name$ serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its functional group containing the triazole moiety allows for selective modifications and controlled reactions, making it a key intermediate in the synthesis of complex organic molecules.One of the primary applications of 4-(1,2,4-Triazol-1-yl)benzyl alcohol is in the synthesis of heterocyclic compounds. The triazole ring in its structure provides a stable and rigid scaffold that can be further functionalized to introduce diverse substituents. This enables chemists to create new compounds with specific biological activities or chemical properties. Additionally, the presence of the benzyl alcohol group offers opportunities for selective transformations, such as oxidation or esterification, enhancing the synthetic versatility of $name$.Moreover, 4-(1,2,4-Triazol-1-yl)benzyl alcohol is utilized in the development of coordination complexes and organometallic compounds. Its coordination ability to various metal ions allows for the formation of metallo-organic complexes with enhanced reactivity and catalytic properties. These complexes find applications in asymmetric catalysis, material science, and medicinal chemistry, highlighting the significance of $name$ in advancing chemical research and development efforts.In summary, the unique structural features and reactivity of 4-(1,2,4-Triazol-1-yl)benzyl alcohol make it a valuable tool in chemical synthesis, enabling the creation of novel compounds with tailored properties and functionalities. Its widespread applications in organic synthesis, heterocyclic chemistry, and coordination chemistry underscore its importance in advancing the frontiers of modern chemical science.