모든 사진(1)
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5 G
₩30,247
About This Item
실험식(Hill 표기법):
C7H5ClN2S
CAS Number:
Molecular Weight:
184.65
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
99%
mp
199-201 °C (lit.)
작용기
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
일반 설명
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[1]. It has synergistic effect on inhibitive performance of propargyl alcohol during corrosion of mild steel in boiling HCl solution[2].
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
이미 열람한 고객
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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