추천 제품
Quality Level
분석
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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애플리케이션
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.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
392.0 °F - closed cup
Flash Point (°C)
200 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
가장 최신 버전 중 하나를 선택하세요:
시험 성적서(COA)
이미 열람한 고객
Preparation of 2-mercaptobenzothiazole-derivatized mesoporous silica and removal of Hg (II) from aqueous solution
Journal of Environmental Monitoring, 8(1), 214-222 (2006)
Sulfur rich 2-mercaptobenzothiazole and 1, 2, 3-triazole conjugates as novel antitubercular agents
European Journal of Medicinal Chemistry, 76, 274-283 (2014)
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
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
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
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