138215
2-氨基-4-甲氧基苯并噻唑
96%
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关于此项目
经验公式（希尔记法）:
C8H8N2OS
化学文摘社编号:
分子量:
180.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-763-1
MDL number:
Assay:
96%
InChI key
YEBCRAVYUWNFQT-UHFFFAOYSA-N
InChI
1S/C8H8N2OS/c1-11-5-3-2-4-6-7(5)10-8(9)12-6/h2-4H,1H3,(H2,9,10)
SMILES string
COc1cccc2sc(N)nc12
assay
96%
mp
153-155 °C (lit.)
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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.
Sareen V, et al.
Phosph. Sulfur Relat. Elem., 185(1), 140-146 (2009)
Antibacterial Zn (II) compounds of. Schiff bases derived from some benzothiazoles.
Chohan ZH and Supuran CT.
Main Group Metal Chemistry, 25(5), 291-296 (2002)
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