472670
氧氟酸
97%
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关于此项目
经验公式（希尔记法）:
C13H9F2NO4
化学文摘社编号:
分子量:
281.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
氧氟酸, 97%
InChI
1S/C13H9F2NO4/c1-5-4-20-12-9(15)8(14)2-6-10(12)16(5)3-7(11(6)17)13(18)19/h2-3,5H,4H2,1H3,(H,18,19)
SMILES string
CC1COc2c(F)c(F)cc3C(=O)C(=CN1c23)C(O)=O
InChI key
NVKWWNNJFKZNJO-UHFFFAOYSA-N
assay
97%
mp
320-322 °C (lit.)
functional group
carboxylic acid
fluoro
ketone
Quality Level
Gene Information
human ... CSNK2A1(1457)
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General description
(S)-(-)-9,10-Difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid may be used in the preparation of the following:
- kynurenine aminotransferase II (KAT II) inhibitor, [(S)-(-)-9-(4-aminopiperazine-1-yl)-8-fluoro-3-methyl-6-oxo-2,3,5,6-tetrahydro-4H-1-oxa-3a-aza-phenalene-5-carboxylic acid]
- fused-ring derivatives
- N-desmethyllevofloxacin
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
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
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Emami S, et al.
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On the relationship between the two branches of the kynurenine pathway in the rat brain in vivo.
Amori L, et al.
Journal of Neurochemistry, 109(2), 316-325 (2009)
Muhammad Malik et al.
Antimicrobial agents and chemotherapy, 54(12), 5214-5221 (2010-09-22)
Quinolones rapidly kill bacteria by two mechanisms, one that requires protein synthesis and one that does not. The latter, which is measured as lethal action in the presence of the protein synthesis inhibitor chloramphenicol, is enhanced by N-1 cyclopropyl and
Andriy G Golub et al.
Journal of medicinal chemistry, 49(22), 6443-6450 (2006-10-27)
Due to the emerging role of protein kinase CK2 as a molecule that participates not only in the development of some cancers but also in viral infections and inflammatory failures, small organic inhibitors of CK2, besides application in scientific research
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