90178-71-5 (4-(4-醛基苯氧基)苯甲腈,4-(4-formylphenoxy)benzonitrile)

CAS号:
90178-71-5
中文名称:
4-(4-醛基苯氧基)苯甲腈
英文名称:
4-(4-formylphenoxy)benzonitrile
安全信息:
分子式:
C14H9NO2
分子量:
223.226763486862

4-(4-醛基苯氧基)苯甲腈(90178-71-5)名称与标识符

名称

中文别名:
4-(4-甲酰苯氧基)苄腈;4-(4-甲酰基苯氧基)苯甲腈;4-(4-醛基苯氧基)苯甲腈;4-(4-氰基苯氧基)苯甲醛;
英文别名:
Benzonitrile, 4-(4-formylphenoxy)-;4-(4-CYANOPHENOXY)BENZALDEHYDE;4-(4-Formylphenoxy)benzonitrile;4-(4-cyano-phenoxy)-benzaldehyde;4-(4-formyl-phenoxy)-benzonitrile;Benzonitrile,4-(4-formylphenoxy);4-(4-Formylphenoxy)benzonitrile (ACI);90178-71-5;W17758;DTXSID40346651;4-[4-Cyanophenoxy]benzaldehyde;AS-8700;4-(4-Formylphenoxy)benzonitrile, 96%;Z335440822;4-(4-Formylphenoxy)benzonitrile #;SCHEMBL505351;CS-0060258;EN300-7360813;DB-078601;4-(4-FORMYLPHENOXY)BENZONITRILE 96;MFCD08276813;AKOS000260457;

标识符

MDL:
MFCD08276813
InChIKey:
PYODQZCRZBCXPW-UHFFFAOYSA-N
Inchi:
1S/C14H9NO2/c15-9-11-1-5-13(6-2-11)17-14-7-3-12(10-16)4-8-14/h1-8,10H
SMILES:
N#CC1C=CC(OC2C=CC(C=O)=CC=2)=CC=1

4-(4-醛基苯氧基)苯甲腈(90178-71-5)物化性质

实验特性

  • LogP : 3.16308
  • PSA : 50.09000
  • 折射率 : 1.615
  • 沸点 : 391.5°C at 760 mmHg
  • 熔点 : 88-93 °C
  • 闪点 : 171.3°C
  • 密度 : 1.24

计算特性

  • 精确分子量 : 223.06300
  • 氢键供体数量 : 0
  • 氢键受体数量 : 3
  • 可旋转化学键数量 : 3
  • 同位素质量 : 223.063328530g/mol
  • 重原子数量 : 17
  • 复杂度 : 291
  • 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) : 2.6
  • 拓扑分子极性表面积 : 50.1Ų

4-(4-醛基苯氧基)苯甲腈(90178-71-5)海关数据

海关编码:
2926909090
海关数据:

中国海关编码:

2926909090

概述:

2926909090 其他腈基化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:6.5% 普通关税:30.0%

申报要素:

品名, 成分含量, 用途

Summary:

HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

4-(4-醛基苯氧基)苯甲腈(90178-71-5)推荐厂家 更多厂家(13)

4-(4-醛基苯氧基)苯甲腈(90178-71-5)合成路线

合成路线:1 步
反应条件:
参考文献:
Discovery of novel cytochrome bc1 complex inhibitor based on natural product neopeltolide
Chen, Tao; Zhang, Rui; Wang, Yu-Xia; Gao, Meng-Qi; Chen, Qiong; et al, Letters in Drug Design & Discovery, 2022, 19(4), 263-268
合成路线:1 步
反应条件:
参考文献:
Ligand-Free Copper-Catalyzed Coupling of Phenols with Nitroarenes by using a Metal-Organic Framework as a Robust and Recoverable Catalyst
Phan, Nam T. S.; Nguyen, Tung T.; Nguyen, Vu T.; Nguyen, Khoa D., ChemCatChem, 2013, 5(8), 2374-2381
合成路线:1 步
反应条件:
参考文献:
Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids
Zhang, Jilei; Chen, Jiuxi; Liu, Miaochang; Zheng, Xingwang; Ding, Jinchang; et al, Green Chemistry, 2012, 14(4), 912-916
合成路线:1 步
反应条件:
参考文献:
Synthesis and Biological Evaluation of Botulinum Neurotoxin A Protease Inhibitors
Li, Bing; Pai, Ramdas; Cardinale, Steven C.; Butler, Michelle M.; Peet, Norton P.; et al, Journal of Medicinal Chemistry, 2010, 53(5), 2264-2276
合成路线:1 步
参考文献:
Syntheses of antimicrobial biscationic 2-(phenoxyphenyl)indoles and -1-benzofurans
Dann, Otto; Ruff, Juergen; Wolff, Hans Peter; Griessmeier, Helmut, Liebigs Annalen der Chemie, 1984, (3), 409-25
合成路线:1 步
反应条件:
参考文献:
Novel benzofuran inhibitors of human mitogen-activated protein kinase phosphatase-1
Lazo, John S.; Nunes, Ruth; Skoko, John J.; Queiroz de Oliveira, Pierre E.; Vogt, Andreas; et al, Bioorganic & Medicinal Chemistry, 2006, 14(16), 5643-5650
合成路线:1 步
反应条件:
参考文献:
19F- and 18F-arene deoxyfluorination via organic photoredox-catalysed polarity-reversed nucleophilic aromatic substitution
Tay, Nicholas E. S. ; Chen, Wei ; Levens, Alison ; Pistritto, Vincent A. ; Huang, Zeng ; et al, Nature Catalysis, 2020, 3(9), 734-742
合成路线:1 步
反应条件:
参考文献:
4-(Phenoxy) and 4-(benzyloxy)benzamides as potent and selective inhibitors of mono-ADP-ribosyltransferase PARP10/ARTD10
Murthy, Sudarshan; Desantis, Jenny; Verheugd, Patricia; Maksimainen, Mirko M.; Venkannagari, Harikanth; et al, European Journal of Medicinal Chemistry, 2018, 156, 93-102
合成路线:1 步
反应条件:
参考文献:
A recyclable Cu-MOF-74 catalyst for the ligand-free O-arylation reaction of 4-nitrobenzaldehyde and phenol
Leo, Pedro; Orcajo, Gisela; Briones, David; Calleja, Guillermo; Sanchez-Sanchez, Manuel; et al, Nanomaterials, 2017, 7(6), 149/1-149/15