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Merck
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文件

M3302

Sigma-Aldrich

2-巯基苯并

97%

别名:

2-苯并噻唑硫醇, MBT

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About This Item

经验公式（希尔记法）:
C7H5NS2
CAS号:
149-30-4
分子量:
167.25
Beilstein:
119484
EC號碼:
205-736-8
MDL號碼:
MFCD00005781
分類程式碼代碼:
12352100
PubChem物質ID:
24896831
NACRES:
NA.22

化驗

97%

mp

177-181 °C (lit.)

SMILES 字串

Sc1nc2ccccc2s1

InChI

1S/C7H5NS2/c9-7-8-5-3-1-2-4-6(5)10-7/h1-4H,(H,8,9)

InChI 密鑰

YXIWHUQXZSMYRE-UHFFFAOYSA-N

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相关类别

應用

2-巯基苯并噻唑（MBT）已被用于合成以MBT进行功能化修饰的介孔二氧化硅，其可用作去除水溶液中Hg（II）的吸附剂。

它也可用作：
  • 在紫外光或可见光照射下光催化活性测试中的参比化合物。
  • 用于抗结核活性研究的2-MBT偶联物合成的起始原料。
  • 合成4-噻唑烷酮的起始原料。

象形圖

Exclamation markEnvironment
GHS07,GHS09

訊號詞

Warning

危險聲明

H317,H410

危險分類

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 2

閃點（°F）

392.0 °F - closed cup

閃點（°C）

200 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Preparation of 2-mercaptobenzothiazole-derivatized mesoporous silica and removal of Hg (II) from aqueous solution
Perez-Quintanilla D, et al.
Journal of Environmental Monitoring, 8(1), 214-222 (2006)
Enhanced photocatalytic activity of Ce3+?TiO2 for 2-mercaptobenzothiazole degradation in aqueous suspension for odour control
Li FB, et al.
Applied Catalysis, 285(1-2), 181-189 (2005)
A facile microwave enhanced synthesis of sulfur-containing 5-membered heterocycles derived from 2-mercaptobenzothiazole over ZnCl2/DMF and antimicrobial activity evaluation
Desai KG, et al.
Journal of Sulfur Chemistry, 27(4), 315-328 (2006)
N Pourreza et al.
Journal of hazardous materials, 178(1-3), 566-571 (2010-02-24)
A novel solid phase extractor for preconcentration of cadmium at ng L(-1) levels has been developed. Cadmium ions were retained on a column packed with sulfur powder modified with 2-mercaptobenzothiazole (2-MBT) in the medium of 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim](+)PF(6)(-)) ionic liquid.
Itai Chipinda et al.
Chemical research in toxicology, 20(8), 1084-1092 (2007-07-17)
The rubber accelerator, 2-mercaptobenzothiazole (MBT), has been reported to cause allergic contact dermatitis from gloves and other rubber products, but its chemical fate when exposed to occupational oxidants and the mechanism of its pathogenesis are not known. It was hypothesized
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