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136085

Sigma-Aldrich

2-Amino-6-chlorobenzothiazole

99%

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About This Item

Empirical Formula (Hill Notation):
C7H5ClN2S
CAS Number:
95-24-9
Molecular Weight:
184.65
EC Number:
202-402-3
MDL number:
MFCD00053557
UNSPSC Code:
12352100
PubChem Substance ID:
24848253
NACRES:
NA.22

Assay

99%

mp

199-201 °C (lit.)

functional group

chloro

SMILES string

Nc1nc2ccc(Cl)cc2s1

InChI

1S/C7H5ClN2S/c8-4-1-2-5-6(3-4)11-7(9)10-5/h1-3H,(H2,9,10)

InChI key

VMNXKIDUTPOHPO-UHFFFAOYSA-N

General description

2-amino-6-chloro-benzothiazole on microwave irradiation in the presence of 1-butyl-3-methylimidazolium and inorganic anions yields fluorinated benzothiazolo[2,3-b]quinazoline-2H-ones analogues. It has synergistic effect on inhibitive performance of propargyl alcohol during corrosion of mild steel in boiling HCl solution.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - 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
MKCQ0673
MKBR8905V
05607BJ
03317MH
18405PR

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Synergistic effect of 2-amino-6-chloro-benzothiazole on inhibitive performance of propargyl alcohol during corrosion of mild steel in boiling hydrochloric acid solution.
Quraishi MA, et al.
Bulletin of Electrochemistry, 13(06), 257-259 (1997)
Jonathan R LaRochelle et al.
Bioorganic & medicinal chemistry, 25(24), 6479-6485 (2017-11-02)
The PTPN11 oncogene encodes the cytoplasmic protein tyrosine phosphatase SHP2, which, through its role in multiple signaling pathways, promotes the progression of hematological malignancies and other cancers. Here, we employ high-throughput screening to discover a lead chemical scaffold, the benzothiazolopyrimidones
Greener synthesis and photo-antiproliferative activity of novel fluorinated benzothiazolo [2, 3-b] quinazolines.
Arya K, et al. et al.
Medicinal Chemistry Research, 1-9 null
Ahmed S M Al-Janabi et al.
Journal of molecular structure, 1228, 129454-129454 (2020-10-27)
New Schiff bases {N'-(phenyl(pyridin-2-yl)methylene) isonicotinohydrazide (L1H), N1 -(naphthalen-1-yl)-N2 -(phenyl(pyridin-2-yl) methylidene) ethane-1,2-diamine (L2H), N-(6-chlorobenzo[d]thiazol-2-yl)-1-phenyl-1-(pyridin-2-yl) methanimine (L3H)}were synthesized by reaction of 2-benzoylpyridine with different amines (2-amino-6-chlorobenzothiazole, isonicotinohydrazide and N 1-(naphthalen-1-yl)ethane-1,2-diamine) and characterized by 1H-NMR, 13C-NMR, IR mass spectroscopy and elemental analysis. The

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