258938
4-甲基-4H-3-巯基-1,2,4-三唑
97%
别名:
3-巯基-4-甲基-4H-1,2,4-三唑
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关于此项目
经验公式（希尔记法）:
C3H5N3S
化学文摘社编号:
分子量:
115.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
246-496-4
Beilstein/REAXYS Number:
110580
MDL number:
Assay:
97%
Form:
solid
产品名称
4-甲基-4H-3-巯基-1,2,4-三唑, 97%
InChI key
AGWWTUWTOBEQFE-UHFFFAOYSA-N
InChI
1S/C3H5N3S/c1-6-2-4-5-3(6)7/h2H,1H3,(H,5,7)
SMILES string
Cn1cnnc1S
assay
97%
form
solid
mp
165-169 °C (lit.)
solubility
acetone: soluble 2.5%, clear, colorless to faintly yellow
Quality Level
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Application
- Corrosion study of mild steel in aqueous sulfuric acid solution using 4-methyl-4H-1, 2, 4-Triazole-3-Thiol: Examines the use of 4-Methyl-4H-1,2,4-triazole-3-thiol as a corrosion inhibitor for mild steel in sulfuric acid solutions (MEHMETI and BERISHA, 2017).
- Dimeric and polymeric mercury (II) complexes containing 4-methyl-1, 2, 4-triazole-3-thiol ligand: Investigates the coordination chemistry of mercury with 4-methyl-4H-1,2,4-triazole-3-thiol, providing insights into its potential applications in materials science (TAHERIHA, GHADERMAZI, and AMANI, 2015).
- Synthesis, characterization and biological studies of 1, 2, 4-triazole derivatives having piperidine moiety: Focuses on the synthesis and biological evaluation of 1,2,4-triazole derivatives, including those modified with a piperidine group and 4-Methyl-4H-1,2,4-triazole-3-thiol (FAROOQ et al., 2023).
General description
4-Methyl-4H-1,2,4-triazole-3-thiol reacts with ethyl bromoacetate to yield ethyl[(4-methyl-4H-1,2,4-triazol-3-yl)sulfanyl]acetate. Electrochemically anticorrosive behavior of self-assembled monolayers of 4-methyl-4H-1,2,4-triazole-3-thiol on the silver electrode has been studied by electrochemical impedance spectroscopy and polarization measurements.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Electrochemical and in situ SERS spectroelectrochemical investigations of 4-methyl-4H-1, 2, 4-triazole-3-thiol monolayers at a silver electrode.
Sun Y, et al.
Journal of Raman Spectroscopy, 40(9), 1306-1311 (2009)
Cyclization of 1-{[(4-Methyl-4H-1, 2, 4-triazol-3-yl) sulfanyl] acetyl} thiosemicarbazides to 1, 2, 4-Triazole and 1, 3, 4-Thiadiazole Derivatives and Their Pharmacological Properties.
Maliszewska-Guz A, et al.
Collection of Czechoslovak Chemical Communications, 70(1), 51-62 (2005)
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