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Merck

136085

Sigma-Aldrich

2-氨基-6-氯苯并噻唑

99%

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About This Item

经验公式(希尔记法):
C7H5ClN2S
CAS号:
分子量:
184.65
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

mp

199-201 °C (lit.)

SMILES 字串

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 密鑰

VMNXKIDUTPOHPO-UHFFFAOYSA-N

一般說明

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.

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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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
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)
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
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

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