- Pd-Catalyzed Autotandem Reactions with N-Tosylhydrazones. Synthesis of Condensed Carbo- and Heterocycles by Formation of a C-C Single Bond and a C=C Double Bond on the Same Carbon AtomParaja, Miguel; Valdes, Carlos, Organic Letters, 2017, 19(8), 2034-2037
Cas no 952709-22-7 (1-Bromo-2-(2-methylphenoxy)benzene)
952709-22-7 structure
Product Name:1-Bromo-2-(2-methylphenoxy)benzene
CAS No:952709-22-7
MF:C13H11BrO
MW:263.129842996597
CID:2111735
Update Time:2023-09-13
1-Bromo-2-(2-methylphenoxy)benzene Chemical and Physical Properties
Names and Identifiers
-
- 1-bromo-2-(2-methylphenoxy)Benzene
- 1-bromo-2-(o-tolyloxy)benzene
- 1-Bromo-2-(2-methylphenoxy)benzene (ACI)
- 1-(2-Bromophenoxy)-2-methylbenzene
- 1-Bromo-2-(2-methylphenoxy)benzene
-
- Inchi: 1S/C13H11BrO/c1-10-6-2-4-8-12(10)15-13-9-5-3-7-11(13)14/h2-9H,1H3
- InChI Key: ATEBZGABNKZVCH-UHFFFAOYSA-N
- SMILES: BrC1C(OC2C(C)=CC=CC=2)=CC=CC=1
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
- Complexity: 195
- Topological Polar Surface Area: 9.2
1-Bromo-2-(2-methylphenoxy)benzene Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Tripotassium phosphate Catalysts: Picolinic acid , Cuprous iodide Solvents: Dimethyl sulfoxide ; 24 h, 110 °C
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Potassium carbonate , Cesium fluoride Solvents: Dimethyl sulfoxide ; 5 h, 50 °C; 50 °C → rt
1.2 Reagents: Stannous chloride Solvents: Ethanol , Water ; 1 h, reflux
1.3 Reagents: Tetrafluoroboric acid Solvents: Diethyl ether , Acetonitrile ; rt → 0 °C; 5 min, 0 °C
1.4 Reagents: tert-Butyl nitrite ; 0 °C; 10 min, 0 °C; 0 °C → -20 °C
1.5 Reagents: Copper bromide (CuBr) , Copper bromide (CuBr2) Solvents: Water ; 0 °C; 2 h, 25 °C
1.2 Reagents: Stannous chloride Solvents: Ethanol , Water ; 1 h, reflux
1.3 Reagents: Tetrafluoroboric acid Solvents: Diethyl ether , Acetonitrile ; rt → 0 °C; 5 min, 0 °C
1.4 Reagents: tert-Butyl nitrite ; 0 °C; 10 min, 0 °C; 0 °C → -20 °C
1.5 Reagents: Copper bromide (CuBr) , Copper bromide (CuBr2) Solvents: Water ; 0 °C; 2 h, 25 °C
Reference
- Preparation of substituted benzoylpiperidine derivatives and analogs as renin inhibitors, World Intellectual Property Organization, , ,
1-Bromo-2-(2-methylphenoxy)benzene Raw materials
1-Bromo-2-(2-methylphenoxy)benzene Preparation Products
1-Bromo-2-(2-methylphenoxy)benzene Related Literature
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Marta Liras,Isabel Quijada-Garrido,Marta Palacios-Cuesta,Sonia Mu?oz-Durieux,Olga García Polym. Chem., 2014,5, 433-442
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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R. M. Pemberton,J. P. Hart,T. T. Mottram Analyst, 2001,126, 1866-1871
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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