InChI
1S/C6H5NO5/c1-11-6(8)4-2-3-5(12-4)7(9)10/h2-3H,1H3
SMILES string
COC(=O)c1ccc(o1)[N+]([O-])=O
InChI key
UTLKCGPAJUYGOM-UHFFFAOYSA-N
assay
98%
mp
78-82 °C (lit.)
Quality Level
General description
Methyl 5-nitro-2-furoate is a nitrofuran derivative. Its density, freezing point and refractive index have been evaluated. The reduction of methyl 5-nitro-2-furoate using milk xanthine oxidase has been reported to form methyl 5-hydroxylamino-2-furoate and methyl 5-amino-2-furoate. The utility of methyl 5-nitro-2-furoate as a matrix compound for matrix assisted ionization vacuum (MAIV) has been assessed using bovine insulin as an analyte.
Application
Methyl 5-nitro-2-furoate may be used in the synthesis of 5-nitro-2-furoylhydrazine and 5-nitro-2-furamide.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Synthesis and antimicrobial activity of methyl 5-nitro-3,4-diphenylfuran-2-carboxylate and related compounds.
Kuo SC, et al.
Chemical & Pharmaceutical Bulletin, 29(3), 635-645 (1981)
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 97-97 (2015)
Reduction of methyl 5-nitro-2-furoate by xanthine oxidase: an evidence for hydroxylaminofuran formation.
H Yamada et al.
Chemical & pharmaceutical bulletin, 30(7), 2647-2650 (1982-07-01)
Syntheses with 5-Nitro-2-furonitrile.
Sherman WR and Esch AV.
Journal of Medicinal Chemistry, 8(1), 25-28 (1965)
Magic matrices for ionization in mass spectrometry.
Trimpin S, et al.
International Journal of Mass Spectrometry, 377, 532-545 (2015)
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