| Identification | More | [Name]
1-BROMO-4-FLUORONAPHTHALENE | [CAS]
341-41-3 | [Synonyms]
1-BROMO-4-FLUORONAPHTHALENE
1-FLUORO-4-BROMONAPHTHALENE
BUTTPARK 44\09-75
1-Bromo-4-fluoronaphthalene,98%
1-Bromo-4-fluoronaphthalene 98%
1-Bromo-4-fluonaphthalene | [EINECS(EC#)]
206-434-9 | [Molecular Formula]
C10H6BrF | [MDL Number]
MFCD00051473 | [Molecular Weight]
225.06 | [MOL File]
341-41-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
35-38 °C (lit.) | [Boiling point ]
110-115 °C(Press: 2 Torr) | [density ]
1.563±0.06 g/cm3(Predicted) | [Fp ]
>230 °F
| [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Chloroform (Slightly), DMSO (Slightly) | [form ]
Solid | [color ]
White | [BRN ]
2085804 | [InChI]
InChI=1S/C10H6BrF/c11-9-5-6-10(12)8-4-2-1-3-7(8)9/h1-6H | [InChIKey]
VAUJZKBFENPOCH-UHFFFAOYSA-N | [SMILES]
C1(Br)=C2C(C=CC=C2)=C(F)C=C1 | [CAS DataBase Reference]
341-41-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29039990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
Solid | [Uses]
1-Bromo-4-fluoronaphthalene is the starting material for the synthesis of Fluorobenzo[c]fluoren (F588435) which is a polycyclic aromatic hydrocarbon used in materials science extensively due to utility in organic electronics, light emitting diodes and solar cells. | [Synthesis]
General procedure for the synthesis of 1-bromo-4-fluoronaphthalene from 1-fluoronaphthalene: 1-fluoronaphthalene (20.0 g, 0.137 mol) was added to a 500 mL single-necked flask with carbon tetrachloride (120.0 mL), and bromine (10.9 g, 0.068 mol) was added dropwise slowly, followed by heating and refluxing for 2 hours. Upon completion of the reaction, the reaction solution was concentrated under reduced pressure and then the concentrate was poured into methanol (80.0 mL). The solid was allowed to precipitate overnight at room temperature to give 28.2 g of 1-bromo-4-fluoronaphthalene in 91.5% yield. | [References]
[1] Patent: CN106478376, 2017, A. Location in patent: Paragraph 0009; 0020; 0021; 0029; 0030; 0038; 0039; 0047
[2] Journal of Medicinal Chemistry, 2004, vol. 47, # 6, p. 1575 - 1586
[3] Justus Liebigs Annalen der Chemie, 1931, vol. 487, p. 270,282
[4] Patent: US2001/49379, 2001, A1
[5] Patent: US6211208, 2001, B1 |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
|
| Telephone: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
Jia Xing Isenchem Co.,Ltd
|
| Telephone: |
0573-85285100 18627885956 |
| Website: |
https://www.chemicalbook.com/ShowSupplierProductsList14265/0_EN.htm |
|