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196061

Sigma-Aldrich

4-Methoxy-3-nitrobenzoic acid

98%

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25 G
R 650,72

R 650,72

List PriceR 664,00
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25 G
R 650,72

About This Item

Linear Formula:
CH3OC6H3(NO2)CO2H
CAS Number:
89-41-8
Molecular Weight:
197.14
EC Number:
201-906-0
MDL number:
MFCD00007256
UNSPSC Code:
12352100
PubChem Substance ID:
24851734
NACRES:
NA.22

R 650,72

List PriceR 664,00
Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

98%

mp

192-194 °C (lit.)

SMILES string

COc1ccc(cc1[N+]([O-])=O)C(O)=O

InChI

1S/C8H7NO5/c1-14-7-3-2-5(8(10)11)4-6(7)9(12)13/h2-4H,1H3,(H,10,11)

InChI key

ANXBDAFDZSXOPQ-UHFFFAOYSA-N

Related Categories

Application

4-Methoxy-3-nitrobenzoic acid was used in the synthesis of:
  • BIPHEP-1-OMe [BIHEP= (2,2′-bis(diphenylphosphino)biphenyl)], precatalyst for reductive coupling of butadiene to aldehydes[1]
  • aniline mustard analogues, having potential anti-tumor activity[2]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
05414LD
13523LR
07125JX
02914DU
08226KY

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Jason R Zbieg et al.
Advanced synthesis & catalysis, 352(14-15), 2416-2420 (2010-12-18)
Exposure of alcohols 1a-1i to butadiene in the presence of a cyclometallated iridium catalyzed derived from allyl acetate, 4-methoxy-3-nitrobenzoic acid and BIPHEP (2,2'-bis(diphenylphosphino)biphenyl) results in hydrogen transfer to generate aldehyde-allyliridium pairs, which engage in C-C coupling to form products of
B G Choi et al.
Archives of pharmacal research, 21(2), 157-163 (1999-01-06)
Several aniline mustard analogues were obtained by introducing N,N-bis(2-chloroethyl)amino moiety to phenyl ring of A10 analogues in order to increase reactivity of A10 analogs and selectivity into DNA. The in vitro antitumor activity of synthesized compounds was evaluated using five

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