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Merck
CN

480509

Methyl 5-nitro-2-furoate

98%

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About This Item

Empirical Formula (Hill Notation):
C6H5NO5
CAS Number:
Molecular Weight:
171.11
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
98%
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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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 97-97 (2015)
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)
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)

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