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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-chloro-1-ethyl-5-methoxy-1H-1,2,4-triazole

COc1nc(nn1CC)Cl Request for Quotation
Chemical Name: 3-chloro-1-ethyl-5-methoxy-1H-1,2,4-triazole
CAS Number: 1330756-30-3
Product Number: AG00J2KM(AGN-PC-0WB619)
Synonyms:
MDL No: MFCD19982739
Molecular Formula: C5H8ClN3O
Molecular Weight: 161.5895

Identification/Properties

Computed Properties
Molecular Weight:
161.589g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
161.036g/mol
Monoisotopic Mass:
161.036g/mol
Topological Polar Surface Area:
39.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
113
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


1H-1,2,4-Triazole, 3-chloro-1-ethyl-5-methoxy- is a versatile chemical compound commonly used in chemical synthesis as a key building block for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential intermediate in the synthesis of diverse organic compounds.In organic synthesis, 1H-1,2,4-Triazole, 3-chloro-1-ethyl-5-methoxy- serves as a valuable precursor for the introduction of functional groups such as ethyl and methoxy substituents into target molecules. These functional groups can significantly influence the physicochemical properties and biological activities of the final products. Additionally, the triazole ring moiety in this compound provides potential sites for further derivatization, allowing the creation of molecular libraries with enhanced properties.Moreover, the presence of the chloro group in the molecule enables selective functionalization reactions, leading to the synthesis of complex molecules with high regioselectivity. This versatility makes 1H-1,2,4-Triazole, 3-chloro-1-ethyl-5-methoxy- a valuable tool in the hands of synthetic chemists for the efficient construction of diverse chemical structures with tailored properties and functionalities.