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4-Bromobutyryl chloride, 97%, Thermo Scientific Chemicals
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Catalog number A12094.22
also known as A12094-22
Price (USD)/ Each
309.65
Online exclusive
344.00 Save 34.35 (10%)
-
Quantity:
100 g
Price (USD)/ Each
309.65
Online exclusive
344.00 Save 34.35 (10%)
4-Bromobutyryl chloride, 97%, Thermo Scientific Chemicals
Catalog numberA12094.22
Price (USD)/ Each
309.65
Online exclusive
344.00 Save 34.35 (10%)
-
Chemical Identifiers
CAS927-58-2
IUPAC Name4-bromobutanoyl chloride
Molecular FormulaC4H6BrClO
InChI KeyLRTRXDSAJLSRTG-UHFFFAOYSA-N
SMILESClC(=O)CCCBr
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥96.0%
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
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.