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Thermo Scientific Chemicals
4-Bromobutyryl chloride, 97%
CAS: 927-58-2 | C4H6BrClO | 185.445 g/mol
化学物質識別子
CAS927-58-2
IUPAC Name4-bromobutanoyl chloride
Molecular FormulaC4H6BrClO
InChI KeyLRTRXDSAJLSRTG-UHFFFAOYSA-N
SMILESClC(=O)CCCBr
さらに表示
仕様
スペックシート
スペックシートFormLiquid
Assay (GC)≥96.0%
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.4900-1.4950 @ 20?C
4-Bromobutyryl chloride is used as a precursor for the synthesis of carolic acid by reacting with ethoxymagnesiomalonic ester. It is widely utilized as an intermediate in organic synthesis and pharmaceuticals.
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-Bromobutyryl chloride is used as a precursor for the synthesis of carolic acid by reacting with ethoxymagnesiomalonic ester. It is widely utilized as an intermediate in organic synthesis and pharmaceuticals.
Solubility
Miscible with organic solvents. Immiscible with water.
Notes
Moisture sensitive. Incompatible with strong oxidizing agents. Remove all sources of ignition. Keep the container tightly closed in a dry and well-ventilated place.
4-Bromobutyryl chloride is used as a precursor for the synthesis of carolic acid by reacting with ethoxymagnesiomalonic ester. It is widely utilized as an intermediate in organic synthesis and pharmaceuticals.
Solubility
Miscible with organic solvents. Immiscible with water.
Notes
Moisture sensitive. Incompatible with strong oxidizing agents. Remove all sources of ignition. Keep the container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
General References:
- Oh, Y. J.; Jeong, C. J.; Sharker, S. M.; Lee, S. Y.; In, I.; Park, S. Y. Synthesis and antibacterial activity of versatile substrate-coated biocidal material via catechol chemistry. Surf. Interface Anal. 2015, 47 (2), 259-264.
- Morotti, A. L. M.; Lang, K. L.; Carvalho, I.; Schenkel, E. P.; Bernardes, L. S. C. Semi-Synthesis of new glycosidic triazole derivatives of dihydrocucurbitacin B. Tetrahedron Lett. 2015, 56 (2), 303-307.