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Home Other Building Blocks 1-Methyl-1H-1,2,4-triazole

1-Methyl-1H-1,2,4-triazole

CAS No.:
6086-21-1
Catalog Number:
AG003EGX
Molecular Formula:
C3H5N3
Molecular Weight:
83.0919
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$25
- +
25g
98%
In Stock USA
United States
$88
- +
100g
98%
In Stock USA
United States
$313
- +
500g
98%
In Stock USA
United States
$1188
- +
Product Description
Catalog Number:
AG003EGX
Chemical Name:
1-Methyl-1H-1,2,4-triazole
CAS Number:
6086-21-1
Molecular Formula:
C3H5N3
Molecular Weight:
83.0919
MDL Number:
MFCD01076192
IUPAC Name:
1-methyl-1,2,4-triazole
InChI:
InChI=1S/C3H5N3/c1-6-3-4-2-5-6/h2-3H,1H3
InChI Key:
MWZDIEIXRBWPLG-UHFFFAOYSA-N
SMILES:
Cn1cncn1
Properties
Complexity:
45.3  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
83.048g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
83.094g/mol
Monoisotopic Mass:
83.048g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
30.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0
Literature
Title Journal
Transformation products of 1,1-dimethylhydrazine and their distribution in soils of fall places of rocket carriers in Central Kazakhstan. The Science of the total environment 20120615
The electronic states of 1,2,4-triazoles: a study of 1H- and 1-methyl-1,2,4-triazole by vacuum ultraviolet photoabsorption and ultraviolet photoelectron spectroscopy and a comparison with ab initio configuration interaction computations. The Journal of chemical physics 20120307
Application of 2-trichloromethylbenzimidazole in analytical chemistry: a highly selective chromogenic reagent for thin-layer chromatography and some other analytical uses. Journal of analytical methods in chemistry 20120101
Structure-activity relationships for NAMI-A-type complexes (HL)[trans-RuCl4L(S-dmso)ruthenate(III)] (L = imidazole, indazole, 1,2,4-triazole, 4-amino-1,2,4-triazole, and 1-methyl-1,2,4-triazole): aquation, redox properties, protein binding, and antiproliferative activity. Journal of medicinal chemistry 20070503
Tuning of redox properties for the design of ruthenium anticancer drugs: part 2. Syntheses, crystal structures, and electrochemistry of potentially antitumor [Ru III/II Cl6-n(Azole)n]z(n = 3, 4, 6) complexes. Inorganic chemistry 20050919
Properties