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258938

Sigma-Aldrich

4-甲基-4H-3-巯基-1,2,4-三唑

97%

同義詞:

3-巯基-4-甲基-4H-1,2,4-三唑

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About This Item

經驗公式(希爾表示法):
C3H5N3S
CAS號碼:
分子量::
115.16
Beilstein:
110580
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

solid

mp

165-169 °C (lit.)

溶解度

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

SMILES 字串

Cn1cnnc1S

InChI

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

InChI 密鑰

AGWWTUWTOBEQFE-UHFFFAOYSA-N

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一般說明

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.

應用

  • 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).

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

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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