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【结 构 式】

【分子编号】66567

【品名】1,2,3,4-tetrahydro-1-naphthoic acid

【CA登记号】1914-65-4

【 分 子 式 】C11H12O2

【 分 子 量 】176.21508

【元素组成】C 74.98% H 6.86% O 18.16%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

 

1 Robinson JR, Kowalczyk JC. 1996. Process for preparing 2-(l-azabicyclo[2, 2, 2] oct-3-yl)-2,3,3a,4, 5,6-hexahydnrlH-benz [de] isoqui nolin-l-one. US 5510486
1 Robinson JR, Kowalczyk JC. 1996. Process for preparing 2-(l-azabicyclo[2. 2, 2] oct-3-yl)-2,3,3a,4,5,6-hexahydnrlH-benz [de] isoqui nolin-l-one. US 5510486
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 16982 1H,3H-benzo[de]isochromene-1,3-dione; 1,8-Naphthalic Anhydride 81-84-5 C12H6O3 详情 详情
(I) 66567 1,2,3,4-tetrahydro-1-naphthoic acid 1914-65-4 C11H12O2 详情 详情
(II) 16985 2-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-1H-benzo[de]isoquinoline-1,3(2H)-dione C19H18N2O2 详情 详情
(II) 27373 1,2,3,4-tetrahydro-1-naphthalenecarbonyl chloride C11H11ClO 详情 详情
(III) 16986 2-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-3-hydroxy-2,3,3a,4,5,6-hexahydro-1H-benzo[de]isoquinolin-1-one C19H24N2O2 详情 详情
(III) 16991 N-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-5,6,7,8-tetrahydro-1-naphthalenecarboxamide 135729-78-1 C18H24N2O 详情 详情
(IV) 16987 2-[(3S)-1-azabicyclo[2.2.2]oct-3-yl]-2,4,5,6-tetrahydro-1H-benzo[de]isoquinolin-1-one C19H22N2O 详情 详情
(IV) 66568 (2S)-N-((1,2,3,4-tetrahydronaphthalen-1-yl)methyl)quinuclidin-2-amine   C18H26N2 详情 详情
Extended Information