Phenoxyacetyl chloride, 98%, Thermo Scientific Chemicals

Description

Acylation of D- and DL-WV with phenoxyacetyl chloride, followed by cleavage of the t-butyl ester,afforded the penultimate penicilloic acids. Phenoxyacetyl chloride was used in the synthesis of series of macrocyclic bis-β-lactams, 5-phenyl-6-epiphenoxymethylpenicillin benzyl ester, N-protected guanosine derivatives, useful in RNA synthesis, phenyloxyketene, for cycloaddition to imines leading to β-lactams. Treatment of iminophosphoranes with phenoxyacetyl chloride afforded respectively the trans- and cis-3-(acylamino)-p-lactams. By the oxidative addition of stannous fluoride to allyliodide, with 1, 2-O-isopropylidene-D-glyceraldehyde and phenoxyacetyl chloride results in the predominant formation of erythro homoallylester, which is in turn converted into 2-deoxy-D-ribose. The 4-disubstituted P-lactams (4a-c and 6a-b) were prepared through the reaction of N,N-diphenylhydrazones and N-methyl-N-phenylhydrazones of ketones with phenoxyacetyl chloride/Et3N in dichloromethane.

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
Acylation of D- and DL-WV with phenoxyacetyl chloride, followed by cleavage of the t-butyl ester,afforded the penultimate penicilloic acids. Phenoxyacetyl chloride was used in the synthesis of series of macrocyclic bis-β-lactams, 5-phenyl-6-epiphenoxymethylpenicillin benzyl ester, N-protected guanosine derivatives, useful in RNA synthesis, phenyloxyketene, for cycloaddition to imines leading to β-lactams. Treatment of iminophosphoranes with phenoxyacetyl chloride afforded respectively the trans- and cis-3-(acylamino)-p-lactams. By the oxidative addition of stannous fluoride to allyliodide, with 1, 2-O-isopropylidene-D-glyceraldehyde and phenoxyacetyl chloride results in the predominant formation of erythro homoallylester, which is in turn converted into 2-deoxy-D-ribose. The 4-disubstituted P-lactams (4a-c and 6a-b) were prepared through the reaction of N,N-diphenylhydrazones and N-methyl-N-phenylhydrazones of ketones with phenoxyacetyl chloride/Et3N in dichloromethane.

Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, moisture.

Specifications

Chemical Identifiers

• CAS: 701-99-5
• Molecular Formula: C8H7ClO2
• Molecular Weight (g/mol): 170.59
• MDL Number: MFCD00000726
• InChI Key: PKUPAJQAJXVUEK-UHFFFAOYSA-N
• Synonym: phenoxyacetyl chloride, acetyl chloride, phenoxy, phenyloxyacetyl chloride, phenoxyacetylchloride, phenoxyacetic acid chloride, acetyl chloride, 2-phenoxy, pac-cl, phenoxylacetylchloride, 2-phenoxyacetylchloride, phenoxy acetyl chloride
• PubChem CID: 69703
• IUPAC Name: 2-phenoxyacetyl chloride
• SMILES: ClC(=O)COC1=CC=CC=C1

• Density: 1.235
• Boiling Point: 225°C to 226°C
• Flash Point: 108°C (226°F)
• Odor: Irritating
• Refractive Index: 1.534
• Quantity: 250 g
• UN Number: UN3265
• Beilstein: 607585
• Sensitivity: Moisture sensitive
• Solubility Information: Reacts with water.
• Formula Weight: 170.6
• Percent Purity: 98%
• Chemical Name or Material: Phenoxyacetyl chloride

RUO – Research Use Only