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93597-01-4 (1-(4-甲氧基苯基)吲哚,1H-Indole, 1-(4-methoxyphenyl)-)

结构式：

1-(4-甲氧基苯基)吲哚结构式图片|93597-01-4结构式图片

1-(4-甲氧基苯基)吲哚MOL文件

CAS号：

93597-01-4

中文名称：

1-(4-甲氧基苯基)吲哚

英文名称：

1H-Indole, 1-(4-methoxyphenyl)-

分子式：

C₁₅H₁₃NO

分子量：

223.269823789597

1-(4-甲氧基苯基)吲哚(93597-01-4)名称与标识符

名称

中文别名：

1-(4-甲氧基苯基)吲哚;

英文别名：

1H-Indole, 1-(4-methoxyphenyl)-;1-(4-Methoxyphenyl)indole;HMS1476I18;BRD-K41860776-001-01-3;DTXSID60354536;93597-01-4;CBDivE_002188;1-(4-methoxy-phenyl)-1h-indole;Cambridge id 5107542;(4-Methoxy-phenyl)1H-indole;SCHEMBL1078090;HMS2879O03;IDI1_020216;1-(4-methoxyphenyl)-1H-indole;CHEMBL1353671;MLS001194500;ChemDiv3_001250;MFCD00541197;AKOS001609193;SMR000555052;CJJDJQFZVLGJLB-UHFFFAOYSA-N;

标识符

InChIKey：

CJJDJQFZVLGJLB-UHFFFAOYSA-N

Inchi：

1S/C15H13NO/c1-17-14-8-6-13(7-9-14)16-11-10-12-4-2-3-5-15(12)16/h2-11H,1H3

SMILES：

O(C)C1C=CC(=CC=1)N1C=CC2C=CC=CC1=2

1-(4-甲氧基苯基)吲哚(93597-01-4)物化性质

计算特性

精确分子量 : 223.099714038g/mol
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 2
同位素质量 : 223.099714038g/mol
重原子数量 : 17
复杂度 : 247
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : 4.3
拓扑分子极性表面积 : 14.2Å²

1-(4-甲氧基苯基)吲哚(93597-01-4)相关文献

1. Metal-free regioselective C-3 acetoxylation of N-substituted indoles: crucial impact of nitrogen-substituent
Vineeta Soni,Ulhas N. Patel,Benudhar Punji RSC Adv. 2015 5 57472
2. N-(1-Oxy-2-picolyl)oxalamic acids as a new type of O,O-ligands for the Cu-catalyzed N-arylation of azoles with aryl halides in water or organic solvent
Yongbin Wang,Yu Zhang,Beibei Yang,Ao Zhang,Qizheng Yao Org. Biomol. Chem. 2015 13 4101
3. A carbon nitride supported copper nanoparticle composite: a heterogeneous catalyst for the N-arylation of hetero-aromatic compounds
Debkumar Nandi,Samarjeet Siwal,Kaushik Mallick New J. Chem. 2017 41 3082
4. Copper-mediated cyanation of indoles and electron-rich arenes using DMF as a single surrogate
Lianpeng Zhang,Ping Lu,Yanguang Wang Org. Biomol. Chem. 2015 13 8322
5. Copper-catalyzed direct coupling of benzoxazin-2-ones with indoles for the synthesis of diverse 3-indolylbenzoxazin-2-ones: access to natural cephalandole A
Rameshwar Prasad Pandit,Jae-Jin Shim,Sung Hong Kim,Yong Rok Lee RSC Adv. 2017 7 55288
6. A convenient eco-friendly system for the synthesis of 5-sulfenyl tetrazole derivatives of indoles and pyrroles employing CeCl3·7H2O in PEG-400
Margiani P. Fortes,Mariana M. Bassaco,Teodoro S. Kaufman,Claudio C. Silveira RSC Adv. 2014 4 34519
7. Efficient Ullmann C–N coupling catalyzed by a recoverable oligose-supported copper complex
Xin Ge,Xinzhi Chen,Chao Qian,Shaodong Zhou RSC Adv. 2016 6 58898
8. Cu(i) based catalysts derived from bidentate ligands and studies on the effect of substituents for N-arylation of benzimidazoles and indoles
Sheela Kumari,Anand Ratnam,Kiran Mawai,Virendra Kumar Chaudhary,Aurobinda Mohanty,Kaushik Ghosh New J. Chem. 2020 44 19591
9. The palladium-catalyzed direct C3-cyanation of indoles using acetonitrile as the cyanide source
Bifu Liu,Min Liu,Qiang Li,Yuanhua Li,Kejun Feng,Yongbo Zhou Org. Biomol. Chem. 2020 18 6108
10. An efficient d-glucosamine-based copper catalyst for C–X couplings and its application in the synthesis of nilotinib intermediate
Ming Wen,Chao Shen,Linfang Wang,Pengfei Zhang,Jianzhong Jin RSC Adv. 2015 5 1522

目录

相关化合物

115552-06-2(9-phenylcarbazol-3-ol) 487058-34-4(6-Methoxy-1-phenyl-1H-indole) 82337-14-2((5Z)-7-[(1α,4α)-3β-[(1E,3S)-3-Hydroxy-1-octenyl]-7-oxabicyclo[2.2.1]heptane-2α-yl]-5-heptenoic acid) 82354-36-7(1,5-Dihydroxy-3-methoxy-10-methyl-4-(3-methyl-2-butenyl)acridin-9(10H)-one) 824409-64-5(4-PIPERAZIN-1-YL-2-TRIFLUOROMETHYL-BENZONITRILE HYDROCHLORIDE) 82430-11-3(dimethyloctanoic acid) 82475-00-1(2-（2,6-二羟基苯基）-5,7-二羟基-4H-色烯-4-酮) 82520-38-5(4-ETHYL-2'-METHOXYBENZOPHENONE)

相关产品

1-(4-甲氧基苯基)吲哚

资讯

广州贝尔卡1-(4-甲氧基苯基)-4-(4-硝基苯基)哌嗪中间体量大从优

问答

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