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1-Bromo-4-fluorobenzene, 99%
1-Bromo-4-fluorobenzene, 99%
1-Bromo-4-fluorobenzene, 99%
Thermo Scientific Chemicals

1-Bromo-4-fluorobenzene, 99%

CAS: 460-00-4 | C6H4BrF | 175.00 g/mol
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数量:
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500 g
2500 g
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製品番号（カタログ番号） A11630.36
または、製品番号A11630-36
価格（JPY）
-
数量:
500 g
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化学物質識別子
CAS460-00-4
IUPAC Name1-bromo-4-fluorobenzene
Molecular FormulaC6H4BrF
InChI KeyAITNMTXHTIIIBB-UHFFFAOYSA-N
SMILESFC1=CC=C(Br)C=C1
さらに表示
仕様Specification Sheetスペックシート
Assay (GC)≥98.5%
Appearance (Color)Clear, colourless
Refractive Index1.5250-1.5280
FormLiquid
Identification (FTIR)Conforms
1-Bromo-4-fluorobenzene is used as an intermediate in the synthesis of atypical antipsychotic agents.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1-Bromo-4-fluorobenzene is used as an intermediate in the synthesis of atypical antipsychotic agents.

Solubility
Soluble in water(0.14g/L).

Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Xi-Bin Gu.; Guang-Jun Wang.; Jian-Hua Huang.; Ke-Li Han.; Guo-Zhong He.; Nan-Quan Lou. Photofragment Translational Spectroscopy of 1-Bromo-3-fluorobenzene and 1-Bromo-4-fluorobenzene at 266 nm. J. Phys. Chem. 2001, 105, (2), 354-362.
  2. Kuniaki Kawataa.; Tsuyoshi Ibarakia.; Akiko Tanabea.; Hiroaki Yagoha.; Akiko Shinodab.; Hiroshi Suzukib.; Akio Yasuhara. Gas chromatographic-mass spectrometric determination of hydrophilic compounds in environmental water by solid-phase extraction with activated carbon fiber felt. Journal of Chromatography A. 2001, 911, (1), 75-83.
  3. The Br undergoes selective displacement with Na alkoxides in NMP, in the presence of CuBr: Tetrahedron, 48, 3633 (1992).
  4. Lithiation with LDA at -75° results mainly in deprotonation ortho to F; subsequent reaction with CO2 gives 5-bromo-2-fluorobenzoic acid: Tetrahedron Lett., 33, 7495 (1992). Improved yields are obtained by the use of Li 2,2,6,6-tetramethylpiperidide (LTMP) as base: Tetrahedron Lett., 37, 6551 (1996).