CAS: 76035-62-6; (2R,4As,6As,6Br,8Ar,10S,12Ar,12Br,14Br)-10-Hydroxy-2,4A,6A,6B,9,9,12A-Heptamethyl-1,2,3,4,4A,5,6,6A,6B,7,8,8A,9,10,11,12,12A,12B,13,14B-Icosahydropicene-2-Carboxylic Acid
该化合物是一种属于有机酸类别的化学化合物,其特点是箱式酸功能组,具有此类化合物典型的酸性与反应性;Epikatonic酸因其在各个领域的潜在应用而著称,包括制药和生物化学,可作为合成更复杂分子的中间体;该化合物一般无色至浅黄色液体或固体,视其特定形式和纯度而定;水和有机溶剂中的溶解性可以不同,在不同化学反应和配方中影响其可用性;此外,它与许多有机酸一样,可能展示生物活动,使其在与药用化学有关的研究中引起兴趣;在处理和储存方面,应参考安全数据,如任何化学物质,以确保对使用该物质可能造成的危险采取适当的防范措施.
- 英文名称(2R,4As,6As,6Br,8Ar,10S,12Ar,12Br,14Br)-10-Hydroxy-2,4A,6A,6B,9,9,12A-Heptamethyl-1,2,3,4,4A,5,6,6A,6B,7,8,8A,9,10,11,12,12A,12B,13,14B-Icosahydropicene-2-Carboxylic Acid
- 中文名称3-表卡通酸
- IUPAC名称(2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid
- 其它别名3-Epikatonic Acid; (20R)-3β-Hydroxyolean-12-En-29-Oic Acid; 3β-Hydroxyoleana-12-Ene-29-Oic Acid; 3-Epicartonic Acid; Olean-12-En-29-Oicacid, 3-Hydroxy-, (3B,20A)-; (3β)-3-Hydroxyolean-12-En-29-Oicaci; Olean-12-En-29-Oic Acid, 3-Hydroxy-, (3β,20α)-
- CAS编号76035-62-6
- 分子式:C30H48O3分子量:456.71
- 产品CID: 1752334
- 产品分类天然产物 → 萜类
物理性质
MSDS等安全信息
上下游产品
enoxolone glycyrrizhin 3β-acetoxy-11-dioxyglycyrrhetic acid diphenylmethyl 11-deoxo-18β-glycyrrhetinate (N-cyclohexyl)-11-deoxyglycyrrhetinic acid amide (4-(trifluoromethyl)benzyl) 3-O-(4-oxo-4H-1-benzopyran-2-carbonyl)-olean-12-en-30-oate (4-bromo-2-fluorobenzyl) 3-O-(4-oxo-4H-1-benzopyran-2-carbonyl)-olean-12-en-30-oate合成工艺路线路线简述
📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于盐酸体系中,用 乙醇,水 作为反应溶剂,化学反应 4.5H,反应生成 3-表卡通酸
参考文献:3-Epikatonic Acid From Guar Meal,Cyamopsis Tetragonoloba
标题:3-Epikatonic Acid From Guar Meal,Cyamopsis Tetragonoloba
摘要:
DOI:10.1016/0031-9422(80)83100-1
海关参考信息
- 2901210000-乙烯
2901220000-丙烯
2905122000-异丙醇
2912110000-甲醛 - 💡 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
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合成参考文献
参考文献:10.1002/mrc.1009
摘要:Silva GDF, Duarte LP, Vieira Filho SA, Doriguetto AC, Mascarenhas YP, Ellena J, Castellano EE, Cota AB. Epikatonic acid from Austroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X‐ray crystallography. Magnetic Reson in Chemistry. 2002 Mar 22;40(5):366–70. doi: 10.1002/mrc.1009.
参考文献:10.4324/9780203304310_chapter_3
摘要:NEEM. CHEMICAL CONSTITUENTS. .
参考文献:10.1016/0031-9422(90)80195-m
摘要:De Sousa JR, Silva GDF, Pedersoli J, Alves RJ. Friedelane and oleanane triterpenoids from bark wood ofAustroplenckia populnea. Phytochemistry. 1990 Jan;29(10):3259–61. doi: 10.1016/0031-9422(90)80195-m.
参考文献:10.1124/mol.119.115964
摘要:Lee TD, Lee OW, Brimacombe KR, Chen L, Guha R, Lusvarghi S, Tebase BG, Klumpp-Thomas C, Robey RW, Ambudkar SV, Shen M, Gottesman MM, Hall MD. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular Pharmacology. 2019 Nov;96(5):629–40. doi: 10.1124/mol.119.115964.
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