中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
对硝基苯甲醛 | 4-nitrobenzaldehdye | 555-16-8 | C7H5NO3 | 151.122 |
—— | 4-methylphenyl(4-nitrophenyl)methanol | 33757-37-8 | C14H13NO3 | 243.262 |
4-硝基苯甲酰氯 | 4-nitro-benzoyl chloride | 122-04-3 | C7H4ClNO3 | 185.567 |
对硝基苯甲酸 | 4-nitro-benzoic acid | 62-23-7 | C7H5NO4 | 167.121 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | 4-(bromomethyl)-4'-nitrobenzophenone | 120712-34-7 | C14H10BrNO3 | 320.142 |
4-(4-硝基苄基)-苯甲酸 | 4-(4-nitrobenzoyl)benzoic acid | 7377-13-1 | C14H9NO5 | 271.229 |
—— | 4-(4-nitrobenzoyl)benzoic acid methyl ester | 79859-23-7 | C15H11NO5 | 285.256 |
—— | (4-((benzyl(methyl)amino)methyl)phenyl)(4-nitrophenyl)methanone | 1298055-70-5 | C22H20N2O3 | 360.412 |
—— | 4-Amino-4'-methylbenzophenone | 6180-80-9 | C14H13NO | 211.263 |
—— | 1-(4-(4-nitrobenzoyl)benzoyl)-3-thiosemicarbazide | 1353654-35-9 | C15H12N4O4S | 344.351 |
—— | 4-methyl-3,4'-dinitro-benzophenone | 99717-09-6 | C14H10N2O5 | 286.244 |
—— | 4-methylphenyl(4-nitrophenyl)methanol | 33757-37-8 | C14H13NO3 | 243.262 |
4-(4-氨基苯甲酰)苯甲酸 | 4-(4-amino-benzoyl)-benzoic acid | 40811-57-2 | C14H11NO3 | 241.246 |
—— | 4'-amino-4-methyl-3-nitro-benzophenone | 860563-99-1 | C14H12N2O3 | 256.261 |
—— | acetic acid-(4-p-toluoyl-anilide) | 6180-81-0 | C16H15NO2 | 253.301 |
—— | 4-(4-aminobenzoyl)benzoic acid methyl ester | 349443-22-7 | C15H13NO3 | 255.273 |
—— | 4-methyl-4'-nitro-benzophenone oxime | 116496-24-3 | C14H12N2O3 | 256.261 |
—— | 1-(diazo(4-nitrophenyl)methyl)-4-methylbenzene | 62147-81-3 | C14H11N3O2 | 253.26 |
—— | (4-aminophenyl)(4-((benzyl(methyl)amino)methyl)phenyl)methanone | 1298055-71-6 | C22H22N2O | 330.429 |
—— | 4-methyl-3-nitrobenzophenone | 79482-00-1 | C14H11NO3 | 241.246 |
—— | 4-methyl-3,3'-dinitro-benzophenone | 873388-64-8 | C14H10N2O5 | 286.244 |
—— | 4-methyl-3,5,4'-trinitro-benzophenone | 331831-18-6 | C14H9N3O7 | 331.241 |
—— | 3-amino-4-methyl-benzophenone | 62261-44-3 | C14H13NO | 211.263 |
A simple, efficient and ligand-free protocol for the Suzuki–Miyaura reaction and base-free Heck–Matsuda reactions under mild reaction conditions has been developed over palladium supported on activated carbon (Pd/C) in an aqueous hydrotropic solution.