M3302
2-Mercaptobenzothiazole
97%
Synonym(s):
2-Benzothiazolethiol, MBT
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About This Item
Empirical Formula (Hill Notation):
C7H5NS2
CAS Number:
Molecular Weight:
167.25
Beilstein:
119484
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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
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Application
2-Mercaptobenzothiazole (MBT) has been used in the synthesis of MBT functionalized mesoporous silica which can be used as an adsorbent for the removal of Hg(II) from aqueous solution.
It can also be used as a:
It can also be used as a:
- Reference compound in photocatalytic activity tests under UV or visible light irradiation.
- Starting material for the synthesis of conjugates of 2-MBT for antitubercular activity studies.
- Starting material for the synthesis of 4-thiazolidinones.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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)
Michael Mah et al.
European journal of orthodontics, 36(6), 657-664 (2013-06-19)
To investigate the different effects of changes in the occlusal plane, incisors inclination, and maxillary intercanine width on the curvature of the smiling line. Records of 46 subjects (28 females and 18 males, mean age 16.6 ± 4.2 years) with
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
H Parham et al.
Journal of hazardous materials, 205-206, 94-100 (2012-01-17)
Mercury in the lowest levels of concentrations is dangerous for human health due to its bioaccumulation in body and toxicity. This investigation shows the effective removal of mercury (II) ions from contaminated surface waters by modified magnetic iron oxide nanoparticles
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)
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