产品名称
2-氨基-5-氯苯并噁唑, 97%
InChI key
YGCODSQDUUUKIV-UHFFFAOYSA-N
InChI
1S/C7H5ClN2O/c8-4-1-2-6-5(3-4)10-7(9)11-6/h1-3H,(H2,9,10)
SMILES string
Nc1nc2cc(Cl)ccc2o1
assay
97%
form
powder
mp
181-184 °C (lit.)
Quality Level
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
K K Anand et al.
Pharmacological research, 36(4), 315-321 (1998-01-13)
Compound I isolated from fraction TB5 of Terminalia belerica and finally identified as 3,4,5-trihydroxy benzoic acid (gallic acid) was evaluated for its hepatoprotective activity against carbon tetrachloride (CCl4)-induced physiological and biochemical alterations in the liver. The main parameters studied were
D J Hadjipavlou-Litina et al.
Research communications in molecular pathology and pharmacology, 96(3), 307-318 (1997-06-01)
Some modified novel thiazol-5yl-aminoketones were evaluated for their anti-inflammatory, analgesic and antiproteolytic activities. Their inhibitory activity on 12-lipoxygenase (12-LO) and beta-glucuronidase in vitro was estimated. Their interaction with the stable free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH) and their RM values were also
Juan P Hernandez et al.
Toxicology and applied pharmacology, 216(2), 186-196 (2006-07-11)
Nonylphenol (NP) is a breakdown product of nonylphenol ethoxylates, which are used in a variety of industrial, agricultural, household cleaning, and beauty products. NP is one of the most commonly found toxicants in the United States and Europe and is
Romi Ghose et al.
Life sciences, 89(1-2), 57-64 (2011-05-31)
Our aim is to investigate the molecular mechanism of regulation of gene expression of drug metabolizing enzymes (DMEs) and transporters in diet-induced obesity. Adult male CD1 mice were fed diets containing 60% kcal fat (HFD) or 10% kcal fat (LFD)
Huidi Jiang et al.
Die Pharmazie, 58(9), 654-656 (2003-10-09)
The present paper aims to investigate whether p-amino-2',4'-dichlorodiphenyl ether and p-amino-4'-methyldiphenyl ether are inhibitors as well as inducers of P450. Mice were given daily intraperitoneal (ip) injections of p-amino-2',4'-dichlorodiphenyl ether (0.25 mmol/kg) or p-amino-4'-methyldiphenyl ether (0.25 mmol/kg) for 4 days
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