missing translation for 'onlineSavingsMsg'
Learn More

Phenoxyacetyl chloride, 98%, Thermo Scientific Chemicals

Product Code. 11494804
Click to view available options
Quantity:
50 g
250 g
1000 g
This item is not returnable. View return policy
This item is not returnable. View return policy

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.
TRUSTED_SUSTAINABILITY

Chemische Identifikatoren

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

Spezifikation

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
Mehr anzeigen Weniger anzeigen

RUO – Research Use Only

Berichtigung von Produktinhalten

Bitte geben Sie uns Ihr Feedback zu den Produktinhalten, indem Sie das folgende Formular ausfüllen.

Name des Produkts

Indem Sie auf Absenden klicken, erklären Sie sich damit einverstanden, dass Fisher Scientific sich mit Ihnen in Verbindung setzen kann, um Ihr Feedback in diesem Formular zu bearbeiten. Wir werden Ihre Informationen nicht für andere Zwecke weitergeben. Alle bereitgestellten Kontaktinformationen werden in Übereinstimmung mit unserer Datenschutzrichtlinie aufbewahrt. Datenschutzrichtlinie.

Vielen Dank, dass Sie uns helfen, unsere Website zu verbessern. Ihr Feedback wurde übermittelt