(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并[b]呋喃-5-基 [1,1’-联苯]-4-甲酸酯

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...基本信息

中文全称

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并[b]呋喃-5-基 [1,1’-联苯]-4-甲酸酯

中文别名

英文名称

(3aR,4R,5R,6aS)-2-Oxo-4-[(1E)-3-oxo-5-phenyl-1-penten-1-yl]hexahy dro-2H-cyclopenta[b]furan-5-yl 4-biphenylcarboxylate

英文别名

ISOALANTOLACTONE (RG);isolantolactone;Naphtho[2,3-b]furan-2(3H)-one,decahydro-8a;ISOHELENIN;methyl-3,5-bis(methylene)-,(3aR,4aS,8aR,9aR);(3ar,4as,8ar,9ar)-8a-methyl-3,5-dimethylene-decahydro-naphtho[2,3-b]furan-2-one;(3aR,4R,5R,6aS)-2-oxo-4-((E)-3-oxo-4-(3-(trifluoromethyl)phenoxy)but-1-en-1-yl)hexahydro-2H-cyclopenta[b]furan-5-yl [1,1'-biphenyl]-4-carboxylate;ISOALANTOACTONE;(3aR,4R,5R,6aS)-2-oxo-4-((E)-3-oxo-4-(3-(trifluoromethyl)phenoxy)but-1-enyl)hexahydro-2H-cyclopenta[b]furan-5-yl biphenyl-4-carboxylate;(3aR,4R,5R,6aS)-4-(3-oxo-5-phenyl-1E-pentenyl)-5-(4-phenylbenzoyloxy)-hexahydro-2H-cyclopenta[b]furan-2-one;(3aR,4R,5R,6aS)-2-oxo-4-((E)-3-oxo-5-phenylpent-1-enyl)hexahydro-2H-cyclopenta[b]furan-5-yl biphenyl-4-carboxylate;(3aR,4aS,8aR,9aR)-decahydro-8a-methyl-3,5-dimethylidenenaphtho[2,3-b]furan-2(3H)-one;[1,1'-biphenyl]-4-carboxylic acid (3aR,4R,5R,6aS)-hexahydro-2-oxo-4-[(1E)-3-oxo-4-[3-(trifluoromethyl)phenoxy]-1-buten-1-yl]-2H-cyclopenta[b]furan-5-yl ester;(1S,5R,6R,7R)-6-(3-oxo-5-phenyl-1E-pentenyl)-7-<(4-phenylbenzoyl)oxy>-2-oxabicyclo<3.3.0>octan-3-one;

PSA

69.67000

LogP

5.58870
(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...物化性质

折射率

1.632

闪点

294.694ºC

密度

1.26

沸点

695.232ºC at 760 mmHg
(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...图谱

核磁图谱

1H NMR : Predict

13C NMR : Predict
(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...合成路线

1.合成路线

1251949-15-1

91%

41639-72-9

参考文献

Zanoni, Giuseppe; D'Alfonso, Alessandro; Porta, Alessio; Feliciani, Lazzaro; Nolan, Steven P.; Vidari, Giovanni Tetrahedron, 2010 , vol. 66, # 38 p. 7472 - 7478

2.合成路线

41639-23-0

89%

41639-72-9

参考文献

Gutman, Arie; Rukhman, Igor; Tishin, Boris; Yudovich, Lev; Vilensky, Alexander; Pertsikov, Boris; Nisnevich, Gennady Patent: US2009/163596 A1, 2009 ; Location in patent: Page/Page column 13-14 ;

3.合成路线

41162-19-0

38754-71-1

72%

41639-72-9

参考文献

Stjernschantz, Johan; Resul, Bahram Patent: US2006/41016 A1, 2006 ; Location in patent: Page/Page column 4 ;
(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...上下游产品

上游产品

41639-23-0

1251949-15-1

31752-99-5
(3aR,4S,5R,6aS)-(-)-六氢-4-(羟甲基)-2-氧代-2H-环戊并[b]呋喃-5-基 1,1'-联苯-4-甲酸酯

41639-72-9
(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并[b]呋喃-5-基 [1,1’-联苯]-4-甲酸酯

下游产品

41639-84-3
(15S)-拉坦前列素游离酸

352276-28-9
拉坦前列腺素内半缩醛

130209-82-4
拉坦前列素

41639-83-2
拉坦前列腺素(游离酸)

上游百科 2-氧代-4-苯丁基磷酸二甲酯对苯基苯甲酰Corey醛 (3aR,4S,5R,6aS)-(-)-六氢-4-(羟甲基)-2-氧代-2H-环戊并[b]呋喃-5-基 1,1'-联苯-4-甲酸酯
下游百科 拉坦前列腺素拉坦前列腺素中间体拉坦前列腺素内半缩醛拉坦前列腺素(游离酸) 拉坦前列腺素

41639-72-9

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...基本信息

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...物化性质

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...图谱

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...合成路线

1.合成路线

1251949-15-1

41639-72-9

2.合成路线

41639-23-0

41639-72-9

3.合成路线

41162-19-0

38754-71-1

41639-72-9

(3aR,4R,5R,6aS)-六氢-2-氧代-4-[(1E)-3-氧代-5-苯基-1-戊烯基]-2H-环戊并...上下游产品

上游产品

下游产品

上游百科

下游百科