84591-12-8 (3,4'-二甲氧基联苯,1,1'-Biphenyl, 3,4'-dimethoxy-)

快速询单

结构式：

3,4'-二甲氧基联苯MOL文件

CAS号：

84591-12-8

中文名称：

3,4'-二甲氧基联苯

英文名称：

1,1'-Biphenyl, 3,4'-dimethoxy-

分子式：

C₁₄H₁₄O₂

分子量：

214.259764194489

3,4'-二甲氧基联苯(84591-12-8)名称与标识符

名称

中文别名：

(6CI,7CI)-3,4’-二甲氧基联苯;3,4'-二甲氧基联苯;

英文别名：

1,1'-Biphenyl, 3,4'-dimethoxy-;1-methoxy-3-(4-methoxyphenyl)benzene;3,4'-DIMETHOXYBIPHENYL;3,4'-Dimethoxy-1,1'-biphenyl;3,4'-Dimethoxy-1,1'-biphenyl #;Biphenyl, 3,4'-dimethoxy- (6CI,7CI);3-methoxy-4'-methoxy-1,1'-biphenyl;SCHEMBL792197;84591-12-8;

标识符

MDL：

MFCD06201373

InChIKey：

FLGIATBXANRPOT-UHFFFAOYSA-N

Inchi：

1S/C14H14O2/c1-15-13-8-6-11(7-9-13)12-4-3-5-14(10-12)16-2/h3-10H,1-2H3

SMILES：

O(C)C1=CC=CC(=C1)C1C=CC(=CC=1)OC

3,4'-二甲氧基联苯(84591-12-8)物化性质

实验特性

熔点 : 60-61 ºC
溶解度 : Very 微溶 (0.11 g/L) (25 ºC),
密度 : 1.056±0.06 g/cm3 (20 ºC 760 Torr),

计算特性

精确分子量 : 214.099379685g/mol
氢键供体数量 : 0
氢键受体数量 : 2
可旋转化学键数量 : 3
同位素质量 : 214.099379685g/mol
重原子数量 : 16
复杂度 : 197
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） : 3.5
拓扑分子极性表面积 : 18.5Å²

3,4'-二甲氧基联苯(84591-12-8)相关文献

1. Electrochemical trifluoromethylation of 2-isocyanobiaryls using CF3SO2Na: synthesis of 6-(trifluoromethyl)phenanthridines
Kannika La-ongthong,Teera Chantarojsiri,Darunee Soorukram,Pawaret Leowanawat,Vichai Reutrakul,Chutima Kuhakarn Org. Biomol. Chem. 2023 21 4225
2. AMVN-initiated expedient synthesis of biaryls by the coupling reaction of unactivated arenes and heteroarenes with aryl iodides
Bhagat Singh Bhakuni,Abhimanyu Yadav,Shailesh Kumar,Sangit Kumar New J. Chem. 2014 38 827
3. Protein–inorganic nano hybrid sheets of Pd embedded BSA as a robust catalyst in water for oxidase mimic activity and C–C coupling reactions, and as a sustainable material for micromolar sensing of dopamine
Sirilata Polepalli,Bhawna Uttam,Chebrolu Pulla Rao Mater. Adv. 2020 1 2074
4. Tandem cyclocondensation of 1,3-bis-sulfonylpropan-2-ones with arylaldehydes. One-pot synthesis of tris-sulfonyl 3-arylphenols
Nai-Chen Hsueh,Meng-Yang Chang Org. Biomol. Chem. 2022 20 8471
5. Reactions of lead tetra-acetate. Part XXI. Acyloxylation, plumbylation, and oxidative dimerisation of some benzenoid compounds in the presence of trifluoro- or trichloro-acetic acid
R. O. C. Norman,C. B. Thomas,J. S. Willson J. Chem. Soc. B 1971 518
6. 981. Biphenylenes. Part VII. Synthesis of 2,3-dimethoxybiphenylene
J. M. Blatchly,J. F. W. McOmie,M. L. Watts J. Chem. Soc. 1962 5085
7. Aromatic substitution. Part XXII. Polarity of aryl radicals
R. A. Abramovitch,O. A. Koleoso J. Chem. Soc. B 1969 779
8. An investigation of the reduction in aqueous acetonitrile of 4-methoxybenzenediazonium ion by the tetrakis(acetonitrile)Cu(i) cation catalysed by hydrogenphosphate dianion
Peter Hanson,Alec B. Taylor,Paul H. Walton,Allan W. Timms Org. Biomol. Chem. 2007 5 679
9. Alternative DNA base-pairs: from efforts to expand the genetic code to potential material applications
Filip Wojciechowski,Christian J. Leumann Chem. Soc. Rev. 2011 40 5669
10. Full theoretical protocol for the design of metal-free organic electron donor–spacer–acceptor systems
Amílcar Duque-Prata,Carlos Serpa,Pedro J. S. B. Caridade Phys. Chem. Chem. Phys. 2023 25 27854