稳定性[10]:稳定。
禁配物[11]:强氧化剂、强还原剂、强酸和强碱。
应避免的条件[12]:受热。
聚合危害[13]:不发生聚合。
分解产物[14]:氮氧化物。
用途:用于有机合成。
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
间硝基苯酚 | meta-nitrophenol | 554-84-7 | C6H5NO3 | 139.111 |
2-甲氧基-4-硝基苯胺 | 2-methoxy-4-nitrophenylamine | 97-52-9 | C7H8N2O3 | 168.152 |
2-硝基-4-甲氧基苯胺 | 4-methoxy-2-nitroaniline | 96-96-8 | C7H8N2O3 | 168.152 |
—— | methyl 3-nitrophenyl carbonate | 17175-17-6 | C8H7NO5 | 197.147 |
1-甲氧基-3-亚硝基苯 | 1-methoxy-3-nitrosobenzene | 26595-63-1 | C7H7NO2 | 137.138 |
4-溴-3-硝基苯甲醚 | 4-bromo-3-nitroanizole | 5344-78-5 | C7H6BrNO3 | 232.034 |
间氨基苯甲醚 | m-Anisidine | 536-90-3 | C7H9NO | 123.155 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
间硝基苯酚 | meta-nitrophenol | 554-84-7 | C6H5NO3 | 139.111 |
4-硝基愈创木酚 | 2-methoxy-4-nitrophenol | 3251-56-7 | C7H7NO4 | 169.137 |
2-甲氧基-4-硝基苯胺 | 2-methoxy-4-nitrophenylamine | 97-52-9 | C7H8N2O3 | 168.152 |
—— | 3-nitrophenyl acetate | 1523-06-4 | C8H7NO4 | 181.148 |
2-硝基-4-甲氧基苯胺 | 4-methoxy-2-nitroaniline | 96-96-8 | C7H8N2O3 | 168.152 |
1-甲氧基-3-亚硝基苯 | 1-methoxy-3-nitrosobenzene | 26595-63-1 | C7H7NO2 | 137.138 |
N-(3-甲氧基苯基)羟胺 | N-(3-methoxyphenyl)hydroxylamine | 24171-80-0 | C7H9NO2 | 139.154 |
4-氯-3-硝基苯甲醚 | 2-chloro-5-methoxynitrobenzene | 10298-80-3 | C7H6ClNO3 | 187.583 |
6-甲氧基-2-硝基苯酚 | 6-methoxy-2-nitrophenol | 15969-08-1 | C7H7NO4 | 169.137 |
4-碘基-3-硝基苯甲醚 | 1-iodo-4-methoxy-2-nitrobenzene | 58755-70-7 | C7H6INO3 | 279.034 |
4-溴-3-硝基苯甲醚 | 4-bromo-3-nitroanizole | 5344-78-5 | C7H6BrNO3 | 232.034 |
2-甲氧基-6-硝基苯胺 | 2-methoxy-6-nitroaniline | 16554-45-3 | C7H8N2O3 | 168.152 |
2-甲氧基-1,4-二硝基-苯 | 2,5-dinitro-anisole | 3962-77-4 | C7H6N2O5 | 198.135 |
1,2-二硝基-4-甲氧基苯 | 3,4-dinitroanisole | 4280-28-8 | C7H6N2O5 | 198.135 |
2-氯甲基-5-硝基茴香醚 | 2-chloromethyl-5-nitro-anisole | 101080-01-7 | C8H8ClNO3 | 201.609 |
—— | 2-methoxy-4-nitro-N-phenylaniline | 82040-92-4 | C13H12N2O3 | 244.25 |
(2-甲氧基-4-硝基苯基)乙腈 | (2-methoxy-4-nitrophenyl)acetonitrile | 313233-24-8 | C9H8N2O3 | 192.174 |
—— | 1-(chloromethyl)-4-methoxy-2-nitrobenzene | 101080-02-8 | C8H8ClNO3 | 201.609 |
—— | 2-methoxy-N-(4-methoxyphenyl)-4-nitroaniline | —— | C14H14N2O4 | 274.276 |
间氨基苯甲醚 | m-Anisidine | 536-90-3 | C7H9NO | 123.155 |
(4-甲氧基-2-硝基苯基)乙腈 | 2-(4-methoxy-2-nitrophenyl)acetonitrile | 105003-90-5 | C9H8N2O3 | 192.174 |
1-甲氧基-2,3-二硝基苯 | 2,3-dinitroanisole | 16315-07-4 | C7H6N2O5 | 198.135 |
2-甲氧基-4-硝基苯甲酸 | 4-nitro-o-anisic acid | 2597-56-0 | C8H7NO5 | 197.147 |
Nanosized perovskite-type SmFeO3 powder, prepared through the thermal decomposition of Sm[Fe(CN)6].4H2O with an average particle diameter of 28 nm and a specific surface area of 42 m2 g−1, was used as a recyclable heterogeneous catalyst for the efficient and selective reduction of aromatic nitro compounds into the corresponding amines by using propan-2-ol as a hydrogen donor (reducing agent) and KOH as a promoter under microwave irradiation. This highly regio- and chemoselective catalytic method is fast, clean, inexpensive, high yielding and also compatible with the substrates containing easily reducible functional groups. In addition, the nanosized SmFeO3 catalyst can be reused without loss of activity.