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Thermo Scientific Chemicals
Acetyl chloride, 98%
CAS: 75-36-5 | C2H3ClO | 78.50 g/mol
化学物質識別子
CAS75-36-5
IUPAC Nameacetyl chloride
Molecular FormulaC2H3ClO
InChI KeyWETWJCDKMRHUPV-UHFFFAOYSA-N
SMILESCC(Cl)=O
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥97.5%
FormLiquid
Identification (FTIR)Conforms
Appearance (Color)Clear colorless to pale pink
Refractive Index1.3875-1.3915 @ 20?C
Acetyl chloride acts as a reagent for the preparation of esters and amides of acetic acid. It is also useful as an important reactant in Friedel-Crafts reactions as well as in the introduction of an acetyl group. It serves as a starting material in the production of pharmaceutical, new plating complexing agent, acylation agent and synthetic organic intermediates.
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
Acetyl chloride acts as a reagent for the preparation of esters and amides of acetic acid. It is also useful as an important reactant in Friedel-Crafts reactions as well as in the introduction of an acetyl group. It serves as a starting material in the production of pharmaceutical, new plating complexing agent, acylation agent and synthetic organic intermediates.
Solubility
Miscible with acetone, chloroform, glacial acetic acid, petroleum ether, ether and benzene.
Notes
Moisture sensitive. Incompatible with water, alcohols, oxidizing agents and strong bases.
Acetyl chloride acts as a reagent for the preparation of esters and amides of acetic acid. It is also useful as an important reactant in Friedel-Crafts reactions as well as in the introduction of an acetyl group. It serves as a starting material in the production of pharmaceutical, new plating complexing agent, acylation agent and synthetic organic intermediates.
Solubility
Miscible with acetone, chloroform, glacial acetic acid, petroleum ether, ether and benzene.
Notes
Moisture sensitive. Incompatible with water, alcohols, oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Indorkar, D.; Chourasia, O. P.; Limaye, S. N. Synthesis and Characterization of some new Synthesis of 1-acetyl-3-(4-nitrophenyl)-5-(substituted phenyl) pyrazoline Derivative and antimicrobial activity. Int. J. Curr. Microbiol. App. Sci. 2015, 4 (2), 670-678.
- Pijper, T. C.; Robertus, J.; Browne, W. R.; Feringa, B. L. Mild Ti-mediated transformation of t-butyl thio-ethers into thio-acetates. Org. Biomol. Chem. 2015, 13 (1), 265-268.