102477-83-8 ((1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-)

快速询单

结构式：

1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-MOL文件

CAS号：

102477-83-8

英文名称：

1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-

分子式：

C₁₅H₁₄O

分子量：

210.271064281464

1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-(102477-83-8)名称与标识符

名称

英文别名：

1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-;1-(4-biphenylphenyl)propan-1-one;biphenyl-4-propiophenone;NSC 24800;1-Propanone,1'-biphenyl]-4-yl-;HMS2571E04;NSC-24800;4-Propionylbiphenyl;1-([1,1'-Biphenyl]-4-yl)propan-1-one;SCHEMBL1928026;NSC24800;UNII-J577D9RAJ8;3-07-00-02183 (Beilstein Handbook Reference);P1212;1-(1,1'-biphenyl-4-yl)propan-1-one;FT-0639422;4-Propanoylbiphenyl;1-[1,1'-Biphenyl]-4-yl-1-propanone #;A823942;1-Propanone, 1-(1,1'-biphenyl)-4-yl- (9CI);p-Phenylpropiophenone;1-(biphenyl-4-yl)propan-1-one;BB 0221156;HMS544C07;DTXSID60191382;SMR000212885;1-Biphenyl-4-yl-propan-1-one;Maybridge1_000931;1-(4-phenylphenyl)propan-1-one;1-Propanone, 1-(1,1'-biphenyl)-4-yl-;SR-01000388912-1;AS-47879;CHEMBL1519521;102477-83-8;SR-01000388912;NCGC00246294-01;J577D9RAJ8;Propiophenone, 4'-phenyl-;BTB 03320;AKOS000161929;MLS000589506;4-Biphenylyl ethylketone;F16654;Ketone, 4-biphenyl ethyl;MFCD00027015;37940-57-1;1-(1,1'-BIPHENYL)-4-YL-1-PROPANONE;4-Phenylpropiophenone;4-Propionylbiphenyl, >/=98%;4'-Phenylpropiophenone;BRN 2047144;WLN: 2VR DR;1-[1,1'-Biphenyl]-4-yl-1-propanone;

标识符

InChIKey：

JMBGDQSXJHLFTO-UHFFFAOYSA-N

Inchi：

1S/C15H14O/c1-2-15(16)14-10-8-13(9-11-14)12-6-4-3-5-7-12/h3-11H,2H2,1H3

SMILES：

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

1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-(102477-83-8)物化性质

实验特性

LogP : 3.94630
PSA : 17.07

计算特性

精确分子量 : 210.10452
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 5
同位素质量 : 286.136
重原子数量 : 22
复杂度 : 328
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） : 4.2
拓扑分子极性表面积 : 17.1A^2

1-Propanone,3-[1,1'-biphenyl]-4-yl-1-phenyl-(102477-83-8)相关文献

1. A fruitful century for the scalable synthesis and reactions of biphenyl derivatives: applications and biological aspects
Hajar A. Ali,Mohamed A. Ismail,Abd El-Aziz S. Fouda,Eslam A. Ghaith RSC Adv. 2023 13 18262
2. CXI.—Optically active β-phthalimino-β-phenylpropiophenones
Alex. McKenzie,Thomas Martin Aitken Tudhope J. Chem. Soc. Trans. 1924 125 923
3. VI.—β-Amino-β-phenylpropiophenone
Alex. McKenzie,Fred Barrow J. Chem. Soc. Trans. 1921 119 69
4. 564. Halogen derivatives of phenyl styryl ketone. Part I. Bromo- and chloro-derivatives
Robert D. Abell,Walter Siddall J. Chem. Soc. 1953 2804
5. Reactions of thiols and sulphides. Part II. Some reactions of sulphur analogues of Mannich bases
F. Poppelsdorf,S. J. Holt J. Chem. Soc. 1954 4094
6. VI.—Natural glucosides. Part I. The constitution of phloridzin
Francis Raban Johnson,Alexander Robertson J. Chem. Soc. 1930 21
7. 94. Grignard reactions with ethyl β-chloropropionate. Part I
Ch. Weizmann,Ernst Bergmann J. Chem. Soc. 1936 401
8. Organic chemistry
J. Chem. Soc. Abstr. 1924 126 i601
9. 93. Hydroxy-carbonyl compounds. Part IX. Benzopyrones related to phloretin
Frederick E. King,Alexander Robertson J. Chem. Soc. 1934 403
10. Reactions of unsaturated acid halides. Part III. Aluminium chloride-catalysed reactions of cinnamoyl chloride with benzene
K. M. Johnston,J. F. Jones J. Chem. Soc. C 1969 814

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