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品質水準
アッセイ
98%
mp
78-82 °C (lit.)
SMILES記法
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
詳細
Methyl 5-nitro-2-furoate is a nitrofuran derivative. Its density, freezing point and refractive index have been evaluated.[1] 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.[2] 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.[3]
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
480509-1KG:
480509-1G:
480509-VAR:
480509-BULK:
480509-5G:
480509-1.2KG:
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
アクティブなフィルタ
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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