- Visible-Light-Promoted, Catalyst-Free Gomberg-Bachmann Reaction: Synthesis of BiarylsLee, Juyoung; Hong, Boseok; Lee, Anna, Journal of Organic Chemistry, 2019, 84(14), 9297-9306
Cas no 154407-17-7 (2-Bromo-3'-chloro-1,1'-biphenyl)
154407-17-7 structure
Product Name:2-Bromo-3'-chloro-1,1'-biphenyl
CAS No:154407-17-7
MF:C12H8BrCl
MW:267.548921585083
CID:4555937
PubChem ID:53701345
Update Time:2024-03-01
2-Bromo-3'-chloro-1,1'-biphenyl Chemical and Physical Properties
Names and Identifiers
-
- 2-bromo-3'-chloro-1,1'-biphenyl
- 1-bromo-2-(3-chlorophenyl)benzene
- 2-Bromo-3'-chloro-1,1'-biphenyl
-
- Inchi: 1S/C12H8BrCl/c13-12-7-2-1-6-11(12)9-4-3-5-10(14)8-9/h1-8H
- InChI Key: CJBHNVDCKKHUFP-UHFFFAOYSA-N
- SMILES: BrC1C=CC=CC=1C1C=CC=C(C=1)Cl
Computed Properties
- Exact Mass: 265.94979 g/mol
- Monoisotopic Mass: 265.94979 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 14
- Rotatable Bond Count: 1
- Complexity: 183
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 5.1
- Topological Polar Surface Area: 0
- Molecular Weight: 267.55
2-Bromo-3'-chloro-1,1'-biphenyl Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Pyridine ; 18 h, 23 °C
Reference
2-Bromo-3'-chloro-1,1'-biphenyl Raw materials
2-Bromo-3'-chloro-1,1'-biphenyl Preparation Products
2-Bromo-3'-chloro-1,1'-biphenyl Related Literature
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1. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
-
Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
-
Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526
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