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454370

Sigma-Aldrich

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:
7442-07-1
Molecular Weight:
182.27
EC Number:
231-184-2
MDL number:
MFCD00059164
UNSPSC Code:
12352100
PubChem Substance ID:
24868576
NACRES:
NA.22

Quality Level

200

Assay

97%

form

solid

mp

267-272 °C (lit.)

SMILES string

Nc1ccc2nc(S)sc2c1

InChI

1S/C7H6N2S2/c8-4-1-2-5-6(3-4)11-7(10)9-5/h1-3H,8H2,(H,9,10)

InChI key

IDPNFKLUBIKHSW-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF4529
BCCD0982
BCCB4910
BCBV6821
BCBT2032

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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)
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)
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

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