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品質等級
化驗
98%
mp
192-194 °C (lit.)
SMILES 字串
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 密鑰
ANXBDAFDZSXOPQ-UHFFFAOYSA-N
應用
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
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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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