W525901
香豆素，日本
别名:
香豆素, 1,2-苯并吡喃酮, 1-苯并吡喃-2-酮, 2H-苯并吡喃-2-酮
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C9H6O2
化学文摘社编号:
分子量:
146.14
EC Number:
202-086-7
UNSPSC Code:
12164502
MDL number:
Beilstein/REAXYS Number:
383644
InChI key
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N
InChI
1S/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H
SMILES string
O=C1Oc2ccccc2C=C1
biological source
synthetic
vapor pressure
0.01 mmHg ( 47 °C)
origin
Japan origin
bp
298 °C (lit.)
mp
68-73 °C (lit.)
正在寻找类似产品? 访问 产品对比指南
Features and Benefits
似新割干草。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Skin Sens. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
323.6 °F - closed cup
flash_point_c
162 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Satoru Tamura et al.
Bioorganic & medicinal chemistry letters, 20(12), 3717-3720 (2010-05-25)
By use of the fission yeast expressing the model fusion protein comprised of GST, SV40 T antigen NLS, GFP, and Rev-NES in the bioassay, the prenylcoumarin osthol (1) was disclosed as the new Rev-export inhibitor from the MeOH extract of
Alfonso Maresca et al.
Bioorganic & medicinal chemistry letters, 20(24), 7255-7258 (2010-11-12)
Two series of disubstituted coumarins incorporating ether and acetyl/propionyl moieties in positions 6,7- and 7,8- of the heterocyclic ring were synthesized investigated for the inhibition of the zinc enzyme carbonic anhydrase (CA, EC 4.2.1.1). All these coumarins were very weak
Kazuto Takaishi et al.
Bioorganic & medicinal chemistry letters, 18(20), 5614-5617 (2008-09-17)
We synthesized all of the monomethoxycoumarins, 5-alkoxycoumarins and their derivatives, and investigated their nematicidal activity against the phytopathogenic nematode, Bursaphelenchus xylophilus. Among the compounds, 5-ethoxycoumarin showed the highest nematicidal activity. Furthermore, 5-ethoxycoumarin was comparatively harmless against both the brine shrimps
Renato F Freitas et al.
Bioorganic & medicinal chemistry, 17(6), 2476-2482 (2009-03-04)
Based on its essential role in the life cycle of Trypanosoma cruzi, the glycolytic enzyme glyceraldehyde 3-phosphate dehydrogenase (GAPDH) has been considered a promising target for the development of novel chemotherapeutic agents for the treatment of Chagas' disease. In the
María E Riveiro et al.
Bioorganic & medicinal chemistry, 17(18), 6547-6559 (2009-09-01)
The presumption that some coumarins might be lead compounds in the search for new differentiation agents against leukemia is based on the fact that natural coumarins, 5-(3-methyl-2-butenyloxy)-6,7-methylenedioxycoumarin (C-2) and 5-methoxy-6,7-methylenedioxycoumarin (C-1) inhibit proliferation and induce differentiation in U-937 cells [Riveiro
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持