454370
6-Amino-2-mercaptobenzothiazole
97%
Synonym(s):
6-Amino-2-benzothiazolethiol
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About This Item
Empirical Formula (Hill Notation):
C7H6N2S2
CAS Number:
Molecular Weight:
182.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
231-184-2
MDL number:
Product Name
6-Amino-2-mercaptobenzothiazole, 97%
InChI key
IDPNFKLUBIKHSW-UHFFFAOYSA-N
InChI
1S/C7H6N2S2/c8-4-1-2-5-6(3-4)11-7(10)9-5/h1-3H,8H2,(H,9,10)
SMILES string
Nc1ccc2nc(S)sc2c1
assay
97%
form
solid
mp
267-272 °C (lit.)
Quality Level
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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[A QSAR study of synthetic stimulators of growth of domestic animals on the basis of 6-amino-2-mercaptobenzothiazole].
P Zahradník et al.
Ceskoslovenska farmacie, 37(10), 440-442 (1988-12-01)
Synthesis and antimicrobial activity of 2-alkylthio-6-aminobenzothiazoles.
Sidoova E, et al.
Chemical Papers, 33, 830-836 (1979)
Electrochemical Characterization of Gold 6-Amino-2-mercaptobenzothiazole Self-Assembled Monolayer for Dopamine Detection in Pharmaceutical Samples.
Shervedani RK, et al.
Electroanalysis, 22(9), 969-977 (2010)
Aiming Sun et al.
ChemMedChem, 6(4), 654-666 (2011-03-03)
Small molecules, namely coactivator binding inhibitors (CBIs), that block estrogen signaling by directly inhibiting the interaction of the estrogen receptor (ER) with coactivator proteins act in a fundamentally different way to traditional antagonists, which displace the endogenous ligand estradiol. To
Triorganotin (IV) complexes of Schiff base derived from 6-amino-2-mercaptobenzothiazole: Synthesis, characterization and X-ray crystal structures.
Ma C, et al.
Inorgorganica Chimica Acta, 360(7), 2439-2446 (2007)
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