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701-99-5 - Phenoxyacetyl chloride, 98% - A13761 - Alfa Aesar

A13761 Phenoxyacetyl chloride, 98%

Numéro CAS
701-99-5
Synonymes

Dimensions Prix ($) Quantité Disponibilité
50g 53,25
250g 170,98
1000g 459,34
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Phenoxyacetyl chloride, 98%

MDL
MFCD00000726
EINECS
211-862-4

Propriétés chimiques

Formule
C8H7ClO2
Poids formulaire
170.60
Point d'ébullition
225-226°
Point d'éclair
108°(226°F)
Densité
1.235
Indice de réfraction
1.5340
Sensibilité
Moisture Sensitive
Solubilité
Reacts with water.

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.

Références bibliographiques

Ajay K. Bose,; J. C. Kapur,; J. L. Fahey,; M. S. Manhas. Lactams. XXIX. Synthesis of aza analogs of cepham . J. Org. Chem., . 1973, 38(19), 3437-3438.

John C. Sheehan,; Kenneth R. Henery-Logan. The Total Synthesis of Penicillin V. J. Am. Chem. Soc., 1959, 81(12), 3089-3094.

Can be used to protect OH groups. The phenoxyacetate group is 50x more labile to aqueous ammonia than acetate: Tetrahedron Lett., 4273 (1968). It can also be cleaved with methanolic t-BuNH 2 : Chem. Lett., 965 (1982).

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H314-H318

Causes severe skin burns and eye damage. Causes serious eye damage.

Mentions de prudence: P260-P280-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P310-P363-P405-P501a

Do not breathe dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Immediately call a POISON CENTER or doctor/physician. Wash contaminated clothing before reuse. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Beilstein
607585
Classe de danger
8
Groupe d'emballage
II
Code tarifaire harmonisé
2918.99
TSCA
Yes

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Catalyseurs

Analytique et matériel de laboratoire