23173-13-9 (（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇,(+/-)-(4aS,6R,8aS)-4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol)

快速询单

结构式：

（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇MOL文件

CAS号：

23173-13-9

中文名称：

（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇

英文名称：

(+/-)-(4aS,6R,8aS)-4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol

分子式：

C₁₇H₂₁NO₃

分子量：

287.354

（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇(23173-13-9)名称与标识符

名称

英文别名：

(+/-)-(4aS,6R,8aS)-4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol;(+/-)-galanthamine;(+/-)galanthamine;(-)-galanthamine;(?)-4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2] benzazepine-6-ol;(?)-galanthamine;1H-(-)-galanthamine;4 a, 5, 9, 10, 11, 12-hexahydro-3- methoxy-11-methyl-6 H-benzofuro-(3 a, 3, 2-ef)-(2) benzazepine-6-ol;4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef]-(2)-benzazepine-6-ol hydrochloride;6-Methoxy-10-methyl-galantham-1-en-3beta-ol;Galanthamin;Hydrochlorid;galanthamine;hydrochloride;Galantamine;Galantamine hydrochloride;Galantamine,INN;galanthamine carbonate;galanthamine hydrochloride;rac-6-methoxy-10-methyl-galantham-1-en-3beta-ol;Reminyl.(R).;Reminyl?;[3H]-Galantamine;

（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇(23173-13-9)相关文献

1. 153. Phenol oxidation and biosynthesis. Part V. The synthesis of galanthamine
D. H. R. Barton,G. W. Kirby J. Chem. Soc. 1962 806
2. Structure and biosynthesis of chlidanthine
J. G. Bhandarkar,G. W. Kirby J. Chem. Soc. C 1970 1224
3. Studies on the syntheses of heterocyclic compounds. Part CCCXV. Modified total synthesis of (±)-galanthamine through phenol oxidation
T. Kametani,K. Yamaki,H. Yagi,K. Fukumoto J. Chem. Soc. C 1969 2602
4. Studies on the syntheses of heterocyclic compounds. Part CCCLXXXVI. Alternative total syntheses of galanthamine and N-benzylgalanthamine iodide
T. Kametani,C. Seino,K. Yamaki,S. Shibuya,K. Fukumoto,K. Kigasawa,F. Satoh,M. Hiiragi,T. Hayasaka J. Chem. Soc. C 1971 1043
5. Amaryllidaceae and Sceletium alkaloids
Zhong Jin Nat. Prod. Rep. 2016 33 1318
6. Stereodivergent routes in organic synthesis: carbohydrates, amino acids, alkaloids and terpenes
Carmen Nájera,Francisco Foubelo,José M. Sansano,Miguel Yus Org. Biomol. Chem. 2020 18 1232
7. Studies on the syntheses of heterocyclic compounds. Part CCCLXXXI. A novel conversion of galanthamine into nivalidine under non-acidic conditions
T. Kametani,K. Yamaki,S. Shibuya,K. Fukumoto,K. Kigasawa,F. Satoh,M. Hiiragi,T. Hayasaka J. Chem. Soc. C 1971 590
8. Studies on the syntheses of heterocyclic compounds. Part CCCLXXXI. A novel conversion of galanthamine into nivalidine under non-acidic conditions
T. Kametani,K. Yamaki,S. Shibuya,K. Fukumoto,K. Kigasawa,F. Satoh,M. Hiiragi,T. Hayasaka J. Chem. Soc. C 1971 590
9. Notes
N. Pravdi?,D. Keglevi?,E. D. Andrews,W. E. Harvey,Roger Bolton,A. F. Casy,J. L. Myers,D. W. Mathiwson,W. B. Whalley,J. M. Blatchly,R. Taylor,A. B. A. Jansen,P. J. Stokes,G. W. H. Cheeseman,J. S. Davidson,J. M. Crabtree,P. N. Gates,E. F. Mooney,J. K. Sutherland,D. A. Widdowson,Stang Mongkolsuk,F. M. Dean,G. W. Kirby,H. P. Tiwari,D. J. Machin,D. F. C. Morris,E. L. Short,R. S. Bluck,A. L. Odell,R. W. Olliff,J. Burdon,W. B. Hollyhead,C. R. Patrick,J. A. Salthouse,T. C. Waddington,Shreekrishna M. Gadedar,Anna Marie Kotsen,Elliott Cohen J. Chem. Soc. 1964 4633
10. Amaryllidaceae and Sceletium alkaloids
John R. Lewis Nat. Prod. Rep. 1996 13 171

791780-06-8(3-(3,4-二氯苯氧基)吖丁啶) 791778-53-5(trans-4-[2-[4-(2,3-Dichlorophenyl)piperazin-1-yl]ethyl]cyclohexanamine) 79201-37-9(4-N-叔丁氧羰基-4-N-甲基氨基哌啶) 787564-37-8((3R)-3-fluoropiperidine;hydrochloride) 78784-70-0(3-CHLORO-6-(2-PYRIDINYLMETHYL)PYRIDAZINE) 78789-65-8(butyl 3-(trichlorostannyl)propanoate compound with 2,2'-bipyridine (1:1) (en)) 792913-82-7((8-甲基-1,4-二氧杂螺[4.5]癸烷-8-基)氨基甲酸叔丁酯) 79324-78-0(1-(3-溴-4-(甲基硫代)苯基)乙酮)

960化工网为您提供（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.23173-13-9,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:23173-13-9 国际站:23173-13-9

23173-13-9 (（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇,(+/-)-(4aS,6R,8aS)-4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol)

（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇(23173-13-9)名称与标识符

名称

（+/-）-（4aS，6R，8aS）-4a，5,9,10,11,12-六氢-3-甲氧基-11-甲基-6H-苯并呋喃[3a，3,2-ef][2]苯并氮杂卓-6-醇(23173-13-9)相关文献

目录