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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)-

1H-1,2,4-Triazole-5-methanol, 1-methyl-

Cn1ncnc1CO Request for Quotation
Chemical Name: 1H-1,2,4-Triazole-5-methanol, 1-methyl-
CAS Number: 91616-36-3
Product Number: AG0036YX(AGN-PC-0CT6EN)
Synonyms:
MDL No:
Molecular Formula: C4H7N3O
Molecular Weight: 113.1179

Identification/Properties

Properties
MP:
66-67℃(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
113.12g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
113.059g/mol
Monoisotopic Mass:
113.059g/mol
Topological Polar Surface Area:
50.9A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
77.7
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Hydroxymethyl-2-methyl-1,2,4-triazole, commonly referred to as $name$, is a versatile compound that finds wide application in chemical synthesis. This compound plays a crucial role as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals.One key application of 3-Hydroxymethyl-2-methyl-1,2,4-triazole is its use as a ligand in coordination chemistry. Due to its unique structure and functional groups, this compound can coordinate with metal ions to form stable complexes. These complexes have been utilized in catalytic processes, such as in the synthesis of heterocyclic compounds and organic transformations.In addition, 3-Hydroxymethyl-2-methyl-1,2,4-triazole is commonly employed as a reagent in organic synthesis. It can participate in various reactions, including condensation, alkylation, and oxidation reactions, to yield compounds of interest. Its ability to function as a nucleophilic and electrophilic agent makes it a valuable tool in the preparation of diverse chemical compounds.Furthermore, this compound has shown promise in the development of novel materials, such as polymers and coordination polymers, due to its ability to form strong hydrogen bonds and engage in supramolecular interactions.Overall, 3-Hydroxymethyl-2-methyl-1,2,4-triazole is a versatile and valuable compound in chemical synthesis, offering unique properties that enable its use in a range of applications across various fields.