추천 제품
Quality Level
분석
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
애플리케이션
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
- aniline mustard analogues, having potential anti-tumor activity
신호어
Warning
유해 및 위험 성명서
예방조치 성명서
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
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
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
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