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Assay
97%
mp
125-130 °C (lit.)
SMILES string
COc1ccc(c(c1)C(O)=O)[N+]([O-])=O
InChI
1S/C8H7NO5/c1-14-5-2-3-7(9(12)13)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)
InChI key
URADKXVAIGMTEG-UHFFFAOYSA-N
Related Categories
General description
5-Methoxy-2-nitrobenzoic acid is a substituted 2-nitrobenzoic acid. It has been reported to be one of the microbial degradation metabolite of cypermethrin, a synthetic pyrethroid pesticide.
Application
5-Methoxy-2-nitrobenzoic acid may be used as starting material in the synthesis of the following:
- dictyoquinazol A, a neuroprotective compound
- 5-methoxyantranilic acid by catalytic reduction
- pyrrolobenzodiazepines
5-Methoxy-2-nitrobenzoic acid may be used in the synthesis of the following N-phenylethyl-2-nitrobenzamides:
- N-phenylethyl-5-methoxy-2-nitrobenzamide
- N-(4-methoxyphenylethyl)-5-methoxy-2-nitrobenzamide
- N-(3,4-dimethoxyphenylethyl)-5-methoxy-2-nitrobenzamide
- N-(phenethyl)-5-chloro-2-nitrobenzamide
- N-(3,4-dimethoxyphenethyl)-5-chloro-2-nitrobenzamide
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis of pyrrolobenzodiazepines via the PIFA oxidation of amines. Synthesis of 8-deoxy DC-81.
Tetrahedron, 54(39), 11749-11754 (1998)
Total synthesis of neuroprotective dictyoquinazol A, B, and C.
Synthetic Communications, 37(19), 3311-3317 (2007)
Biodegradation of Hazardous and Special Products (Intech), 1-16 (2013)
A Novel Synthesis of 5, 6-Dihydroindazolo [3,2-a] isoquinolines and Their Relative Compounds via Tin (II) Chloride Dihydrate as Reducing Agent.
J. Chin. Chem. Soc., 52(5), 965-974 (2005)
Derivatives of 6-methoxy-2-mercaptoquinazole-4-one as compounds with potential anti-tubercularactivity.
Pharmaceutical Chemistry Journal, 1(8), 456-458 (1967)
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