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质量水平
方案
98%
mp
78-82 °C (lit.)
SMILES字符串
COC(=O)c1ccc(o1)[N+]([O-])=O
InChI
1S/C6H5NO5/c1-11-6(8)4-2-3-5(12-4)7(9)10/h2-3H,1H3
InChI key
UTLKCGPAJUYGOM-UHFFFAOYSA-N
一般描述
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.
应用
Methyl 5-nitro-2-furoate may be used in the synthesis of 5-nitro-2-furoylhydrazine and 5-nitro-2-furamide.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
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)
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)
Magic matrices for ionization in mass spectrometry.
Trimpin S, et al.
International Journal of Mass Spectrometry, 377, 532-545 (2015)
H Yamada et al.
Archives of biochemistry and biophysics, 232(1), 234-239 (1984-07-01)
After methyl 5-nitro-2-furoate was incubated with milk xanthine oxidase, three reduction products were isolated from the incubation mixture. Among them, two reduction products were new types of nitrofuran metabolites, i.e., metabolites 1 and 2 were identified as the dihydroxyhydrazine derivative
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