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Sigma-Aldrich

5-Methoxy-2-nitrobenzoic acid

97%

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About This Item

Linear Formula:
CH3OC6H3(NO2)CO2H
CAS Number:
1882-69-5
Molecular Weight:
197.14
MDL number:
MFCD00151836
UNSPSC Code:
12352100
PubChem Substance ID:
24864416
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

assay

97%

mp

125-130 °C (lit.)

functional group

carboxylic acid
nitro

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

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antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

rabbit

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

-

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

Prestige Antibodies® Powered by Atlas Antibodies

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

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.[1]

Application

5-Methoxy-2-nitrobenzoic acid may be used as starting material in the synthesis of the following:
  • dictyoquinazol A, a neuroprotective compound[2]
  • 5-methoxyantranilic acid by catalytic reduction[3]
  • pyrrolobenzodiazepines[4]
5-Methoxy-2-nitrobenzoic acid may be used in the synthesis of the following N-phenylethyl-2-nitrobenzamides:[5]
  • 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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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    Certificates of Analysis (COA)

    Lot/Batch Number
    S37679
    10617EE
    13113CE
    06229PD
    08327LC

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    Derivatives of 6-methoxy-2-mercaptoquinazole-4-one as compounds with potential anti-tubercularactivity.
    Murav'eva KM, et al.
    Pharmaceutical Chemistry Journal, 1(8), 456-458 (1967)
    Total synthesis of neuroprotective dictyoquinazol A, B, and C.
    Oh CH and Song CH.
    Synthetic Communications, 37(19), 3311-3317 (2007)
    Yin LB, et al.
    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.
    Kuo CY and Wu MJ.
    J. Chin. Chem. Soc., 52(5), 965-974 (2005)
    Synthesis of pyrrolobenzodiazepines via the PIFA oxidation of amines. Synthesis of 8-deoxy DC-81.
    Kraus GA and Melekhov A.
    Tetrahedron, 54(39), 11749-11754 (1998)

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