M3302
2-巯基苯并
97%
别名:
2-苯并噻唑硫醇, MBT
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关于此项目
经验公式（希尔记法）:
C7H5NS2
化学文摘社编号:
分子量:
167.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-736-8
Beilstein/REAXYS Number:
119484
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
177-181 °C (lit.)
SMILES string
Sc1nc2ccccc2s1
InChI
1S/C7H5NS2/c9-7-8-5-3-1-2-4-6(5)10-7/h1-4H,(H,8,9)
InChI key
YXIWHUQXZSMYRE-UHFFFAOYSA-N
Application
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：
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。
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
392.0 °F - closed cup
flash_point_c
200 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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)
Sulfur rich 2-mercaptobenzothiazole and 1, 2, 3-triazole conjugates as novel antitubercular agents
Mir F, et al.
European Journal of Medicinal Chemistry, 76, 274-283 (2014)
Fei Wang et al.
Organic letters, 13(12), 3202-3205 (2011-05-20)
An efficient strategy for the synthesis of a variety of 2-mercaptobenzothiazole derivatives has been developed. The reaction proceeded from o-haloaniline derivatives and carbon disulfide via a tandem reaction in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) to afford the corresponding 2-mercaptobenzothiazole derivatives
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| M3302-100G | 04061834050100 |
| M3302-1KG | 04061834050117 |
| M3302-5G | 04061834050124 |