Recommended Products
Assay
96%
mp
153-155 °C (lit.)
SMILES string
COc1cccc2sc(N)nc12
InChI
1S/C8H8N2OS/c1-11-5-3-2-4-6-7(5)10-8(9)12-6/h2-4H,1H3,(H2,9,10)
InChI key
YEBCRAVYUWNFQT-UHFFFAOYSA-N
Biochem/physiol Actions
2-Amino-4-methoxybenzothiazole on condensation reaction with 4-acetamidobenzaldehyde affords tridentate Schiff bases. It reacts with 2,4,6-trichloro 1,3,5-triazine to give 2-(4-methoxybenzothiazol-2′-ylamino)-4-(phenylthioureido)-6-(substitutedthioureido)-1,3,5-triazines.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
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
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of Some New 2-(4-Methoxybenzothiazol-2'-yl amino)-4-(2-chloro-4-trifluoromethylanilino)-6-(substituted thioureido)-1, 3, 5-triazine as Antifungal Agents.
Phosph. Sulfur Relat. Elem., 185(1), 140-146 (2009)
Antibacterial Zn (II) compounds of. Schiff bases derived from some benzothiazoles.
Main Group Metal Chemistry, 25(5), 291-296 (2002)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service