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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

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

454370-VAR:
454370-BULK:
454370-1G:
454370-5G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Synthesis and antimicrobial activity of 2-alkylthio-6-aminobenzothiazoles.
Sidoova E, et al.
Chemical Papers, 33, 830-836 (1979)
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
[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)

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