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Merck
CN
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文件

258938

Sigma-Aldrich

4-甲基-4H-3-巯基-1,2,4-三唑

97%

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别名:
3-巯基-4-甲基-4H-1,2,4-三唑
经验公式（希尔记法）:
C3H5N3S
CAS号:
24854-43-1
分子量:
115.16
Beilstein:
110580
EC 号:
246-496-4
MDL编号:
MFCD00010069
UNSPSC代码:
12352100
PubChem化学物质编号:
24855670
NACRES:
NA.22

质量水平

100

检测方案

97%

形式

solid

mp

165-169 °C (lit.)

溶解性

acetone: soluble 2.5%, clear, colorless to faintly yellow

SMILES字符串

Cn1cnnc1S

InChI

1S/C3H5N3S/c1-6-2-4-5-3(6)7/h2H,1H3,(H,5,7)

InChI key

AGWWTUWTOBEQFE-UHFFFAOYSA-N

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相关类别

一般描述

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.

应用

  • 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).

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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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)
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)

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