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Thermo Scientific Chemicals
(4-Bromobutoxy)benzene, 97%
CAS: 1200-03-9 | C10H13BrO | 229.12 g/mol
化学物質識別子
CAS1200-03-9
IUPAC Name(4-bromobutoxy)benzene
Molecular FormulaC10H13BrO
InChI KeyQBLISOIWPZSVIK-UHFFFAOYSA-N
SMILESBrCCCCOC1=CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White to brown
FormCrystals or powder or crystalline powder or lumps or fused solid
Melting Point (clear melt)36.0-46.0?C
Assay (GC)≥96.0%
(4-Bromobutoxy)benzene is used to produce 5-phenoxy-valeric acid with carbon dioxide and reagent Mg.
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
(4-Bromobutoxy)benzene is used to produce 5-phenoxy-valeric acid with carbon dioxide and reagent Mg.
Solubility
Insoluble in water.
Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
(4-Bromobutoxy)benzene is used to produce 5-phenoxy-valeric acid with carbon dioxide and reagent Mg.
Solubility
Insoluble in water.
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:
- Ryoji Kikumoto.; Akihiro Tobe.; Shinji Tonomura. Synthesis and antidepressant activity of substituted (.μ.-aminoalkoxy)benzene derivatives. J. Med. Chem. 1981, 24, (2), 145-148.
- William T. Brady.; Yun Seng F. Giang.; Lingling Weng.; Mohammad M. Dad. Intramolecular [2 + 2] cycloadditions of ketene iminium salts to carbon-carbon double bonds. J. Org. Chem. 1987, 52, (11), 2216-2220.