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Thermo Scientific Chemicals
Iodoacetyl chloride, 97%
CAS: 38020-81-4 | C2H2ClIO | 204.39 g/mol
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化學識別
CAS38020-81-4
IUPAC Name2-iodoacetyl chloride
Molecular FormulaC2H2ClIO
InChI KeyBSVMPWANOMFSPR-UHFFFAOYSA-N
SMILESClC(=O)CI
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規格
規格表
規格表FormLiquid
Assay (GC)≥96.0%
Appearance (Color)Clear dark red to red to brown to black
Assay (Titration ex Chloride)≥96.0 to ≤104.0%
Iodoacetyl chloride is used for biochemical research purposes.
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
Iodoacetyl chloride is used for biochemical research purposes.
Solubility
Miscible with water.
Notes
Moisture and light sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, strong bases and strong reducing agents. Reacts with water.
Iodoacetyl chloride is used for biochemical research purposes.
Solubility
Miscible with water.
Notes
Moisture and light sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, strong bases and strong reducing agents. Reacts with water.
RUO – Research Use Only
General References:
- Tavenor, N. A.; Silva, K. I.; Saxena, S.; Horne, W. S. Origins of Structural Flexibility in Protein-Based Supramolecular Polymers Revealed by DEER Spectroscopy. J. Phys. Chem. B 2014, 118 (33), 9881-9889.
- Zhao, R.; Sun, Z.; Mo, M.; Peng, F.; Shao, Z. Catalytic Asymmetric Assembly of C3-Monosubstituted Chiral Carbazolones and Concise Formal Synthesis of (-)-Aspidofractinine: Application of Enantioselective Pd-Catalyzed Decarboxylative Protonation of Carbazolones. Org. Lett. 2014, 16 (16), 4178-4181.