CAS: 93457-07-9; 2,4-Dichlorophenylacetone
该化合物是一种有机化合物,其特点是其氯酮功能组和二氯苯替代成分,一般视温度和纯度而定,其颜色无色可粉黄液体或固体,因其独特的气味而闻名,并经常用于有机合成和作为生产各种化学品的中间体,其分子结构包括一个2,4-二氯苯组的丙酮脊椎,有助于其再活性和在制药和农用化学品中的潜在应用.氯原子的存在会加强其生物活动,并影响其溶性在不同溶剂中的溶性与稳定性.与许多有机化合物一样,在处理时应注意安全防范,因为如果吸入或摄入,可能会对健康造成危害.适当的储存条件对于保持其完整性和防止降解至关重要.
- 英文名称2,4-Dichlorophenylacetone
- 中文名称2,4-二氯苯基丙酮
- IUPAC名称1-(2,4-dichlorophenyl)propan-2-one
- 其它别名1-(2,4-Dichlorophenyl)-2-Propanone; Physodicacid; Itvvhxzqwsczbc-Uhfffaoysa-N; 1-(2,4-Dichlorophenyl)-Propan-2-One; 1-(2,4-D
- CAS编号93457-07-9
- MFCD编号:MFCD00210405
- 分子式:C9H8Cl2O分子量:203.07
- 产品CID: 1974124
- 产品分类化学试剂 → 有机试剂 → 芳香酮
物理性质
MSDS等安全信息
上下游产品
2-(2,4-Dichlorophenyl)-N-methoxy-N-methylacetamide methylmagnesium bromide 2-(2,4-dichloro-phenyl)-1-methyl-ethylamine 1,3-Dibromo-1-(2,4-dichloro-phenyl)-propan-2-one 3-(2,4-Dichloro-phenyl)-3-hydroxy-4-[1,2,4]triazol-1-yl-butan-2-one (Z)-3-(2,4-Dichloro-phenyl)-acrylic acid methyl ester合成工艺路线路线简述
- 691411-77-5 = 93457-07-9
反应条件:1.1 Solvents: Methanol,Toluene; 30 Min,-78 °C; 1 H,Rt1.2 Reagents: Ammonium Chloride Solvents: Water; Rt
标题:Allosteric Regulation Of Hsp90α'S Activity By Small Molecules Targeting The Middle Domain Of The Chaperone
作者:Zhou,Chen; Zhang,Chi; Zhu,Hongwen; Liu,Zhijun; Su,Haixia; Et Al
参考文献:Iscience 日期:2020 卷标:23(2)]
691411-77-5 = 93457-07-9
反应条件:1.1 Solvents: Toluene,Tetrahydrofuran; -78 °C -> Rt; 30 Min,Rt; Rt -> 0 °C1.2 Reagents: Ammonium Chloride Solvents: Water; 0 °C
标题:Preparation Of Cyanothiophene Derivatives As Glucagon Antagonists For Treating Type Ii Diabetes Mellitus
参考文献:United States]
= 93457-07-9 [标题:Reaction Conditions
标题:Synthesis Of Benzylic Ketones And Alcohols By Electroreductive Coupling Of Benzylic Compounds Bearing A Leaving Group Other Than A Halogen With Anhydrides And Carbonyl Compounds
作者:Gal,J.; Folest,J. C.; Troupel,M.; Guitton,P.; Robin,Y.
参考文献:New Journal Of Chemistry 日期:1996 卷标:20(3) 页码:375-83]
108-22-5 + 554-00-7 = 93457-07-9
反应条件:1.1 Reagents: Sodium Nitrite,Hydrochloric Acid Solvents: Water; 45 Min,-5 °C; 15 Min,-5 °C1.2 Reagents: Hydrofluoric Acid,Boric Acid (H3Bo3); 30 Min,-5 °C; 2 H,0 °C1.3 Reagents: Sodium Acetate Catalysts: Copper Oxide (Cu2O); 30 Min,20 - 25 °C; 6 H,20 - 25 °C
标题:Synthesis And Fungicidal Activity Of Novel Oxathiapiprolin Derivatives
作者:Ding,Chengrong; Pan,Yayun; Yin,Xu; Tan,Chengxia; Wang,Xuedong
参考文献:Youji Huaxue 日期:2019 卷标:39(7) 页码:2062-2069]
127138-62-9 = 93457-07-9
反应条件:1.1 Catalysts: Acetic Anhydride
标题:Electrosynthesis Of Benzylic Ketones
参考文献:France]
= 93457-07-9 [标题:Reaction Conditions
标题:Synthesis And Biological Activity Of Thiazolidine Piperidine Nicotinamide Compounds
作者:Ding,Chengrong; Pan,Yayun; Yin,Xu; Tan,Chengxia
参考文献:Youji Huaxue 日期:2019 卷标:39(7) 页码:2099-2105
📜(2,4-Dichlorophenyl)Methyl-Trimethylazanium;Iodide,乙酸酐 以50%的收率获得产物
参考文献:Robin,Yves;Chaussard,Jacques;Troupel,Michel;Guitton,Pascale
标题:Robin,Yves;Chaussard,Jacques;Troupel,Michel;Guitton,Pascale
海关参考信息
- 2902600000-乙苯
2903919090-氯苯
2912110000-甲醛
2912120000-乙醛 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:EP-3590340-B1
优先权日:2010-09-01
标 题:Intermediates for the synthesis of fungicidal pyrazoles
专利号:ES-2971524-T3
优先权日:2010-09-01
标 题 :Intermediates for the synthesis of fungicide pyrazoles
