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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-1,2,3-Triazole, 1-methyl-

Cn1ccnn1 Request for Quotation
Chemical Name: 1H-1,2,3-Triazole, 1-methyl-
CAS Number: 16681-65-5
Product Number: AG0035Z0(AGN-PC-0CZUIV)
Synonyms:
MDL No:
Molecular Formula: C3H5N3
Molecular Weight: 83.0919

Identification/Properties

Properties
BP:
149.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
83.094g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
83.048g/mol
Monoisotopic Mass:
83.048g/mol
Topological Polar Surface Area:
30.7A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
45.3
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-1,2,3-triazole is a versatile building block in chemical synthesis, known for its unique reactivity and wide range of applications. This compound serves as a valuable precursor in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its ability to participate in diverse chemical transformations.One key application of 1-Methyl-1,2,3-triazole is as a ligand in coordination chemistry, where it can coordinate to metal ions and enhance catalytic reactions. This compound is also utilized in the synthesis of heterocyclic compounds, such as triazole derivatives, which exhibit interesting biological activities and serve as important intermediates in drug discovery.Furthermore, 1-Methyl-1,2,3-triazole plays a crucial role in the preparation of functionalized polymers and advanced materials. Its presence in these materials imparts unique properties and functionalities, making them suitable for various industrial applications.Overall, the versatility and reactivity of 1-Methyl-1,2,3-triazole make it a valuable tool in chemical synthesis, enabling the development of diverse compounds with applications across different sectors of the chemical industry.