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4-Bromobutyronitrile, 97%
CAS: 5332-06-9 | C4H6BrN | 148.00 g/mol
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Catalog number A10674.18
also known as A10674-18
Price (EUR)
138,00
Each
Quantity:
50 g
Price (EUR)
138,00
Each
Chemical Identifiers
CAS5332-06-9
IUPAC Name4-bromobutanenitrile
Molecular FormulaC4H6BrN
InChI KeyCQPGDDAKTTWVDD-UHFFFAOYSA-N
SMILESBrCCCC#N
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to pale yellow
CommentMaterial sourced in the U.S. and in other countries
Refractive Index1.4755-1.4805 @ 20°C (non-U.S. sourced material)
Assay (GC)≥96.0%
FormLiquid
4-bromobutyronitrile is used as a precursor for the preparation of cylopropyl cyanide. Its derivative, 4-Bromo-2,2-Diphenyl Butyronitrile is used as an intermediate for loperamide.
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-bromobutyronitrile is used as a precursor for the preparation of cylopropyl cyanide. Its derivative, 4-Bromo-2,2-Diphenyl Butyronitrile is used as an intermediate for loperamide.
Solubility
Miscible with toluene and benzene. Immiscible with water.
Notes
Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong acids, strong bases, strong oxidizing agents and strong reducing agents.
4-bromobutyronitrile is used as a precursor for the preparation of cylopropyl cyanide. Its derivative, 4-Bromo-2,2-Diphenyl Butyronitrile is used as an intermediate for loperamide.
Solubility
Miscible with toluene and benzene. Immiscible with water.
Notes
Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong acids, strong bases, strong oxidizing agents and strong reducing agents.
RUO – Research Use Only
General References:
- Sahiner, N.; Atta, A. M.; Yasar, A. O.; Al-Lohedan, H. A.; Ezzat, A. O. Surface activity of amphiphilic cationic pH-responsive poly(4-vinylpyridine) microgel at air/water interface. Colloids Surf. A 2015, 482, 647-655.
- Asekunowo, P. O.; Haque, R. A. Counterion-induced modulation in biochemical properties of nitrile functionalized silver(I)-N-heterocyclic carbene complexes. J. Coord. Chem. 2014, 67 (22), 3469-34663.