| Weight | 169.636 g/mol |
|---|---|
| Formula | C7H4ClNS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2-Chlorobenzothiazole (615-20-3)
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- Copper(II) Polyamine Complexes with N-Benzothiazole Sulfonamides as Counterions Synthesis, Crystal Structures, and Properties of [Cu(dien)2](L1)2[HL1 = N-2-(benzothiazole)naphtalenesulfonamide, dien = diethylentriamine] and [Cu(en)2(H2O)2](L2)2[HL2 = N-2-(6-chlorobenzothiazole)toluenesulfonamide, en = ethylenediamine] Superoxide Dismutase-like Activity (Zeitschrift fr anorganische und allgemeine Chemie, 2003)
- Interaction of 2-Chlorobenzothiazole with Aromatic Thiocarbamides. I. Formation of Guanylthiocarbamides and Sulfides (Journal of Organic Chemistry, 1963)
- Cross-coupling of 2-chlorobenzothiazole with benzothiazolylalkyl-magnesium bromide: synthesis of bis(2-benzothiazolyl)alkanes (Heterocycles, 1986)
- The Kinetics of the Ammonolysis of 2-Chlorobenzothiazole by Liquid Ammonia (Journal of the American Chemical Society, 1941)
- Synthesis of New Antimicrobials. III. Synthesis of Chlorine-substituted 4-Thiocyanatoaniline and 2-Amino-6-chlorobenzothiazole Derivatives (Chemical & Pharmaceutical Bulletin, 1975)
- Diazotization of 2,6-diaminobenzothiazole: A new process for the preparation of 2-chlorobenzothiazole reactive azo dyes (Dyes and Pigments, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)N=C(S2)Cl
-
InChIKeyBSQLQMLFTHJVKS-UHFFFAOYSA-N
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Similar Compounds
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2-Chlorobenzothiazole
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