Phenoxyacetylchlorid

Phenoxyacetyl chloride

HCID 69703CAS 701-99-5

Grundinformationen

Standard-SMILES
O=C(Cl)COc1ccccc1
InChIKey
PKUPAJQAJXVUEK-UHFFFAOYSA-N
Summenformel
C8H7ClO2
Durchschnittliche Molmasse
170,59 g/mol
Monoisotopische Masse
170,01345714

Namen und Bezeichner

Bevorzugter Name
Phenoxyacetyl chloride
IUPAC
2-phenoxyacetyl chloride
Lokaler Name
Phenoxyacetylchlorid
Englischer Name
Phenoxyacetyl chloride
Summenformel
C8H7ClO2
Molmasse
170.59

Namen und Synonyme

Phenoxyacetyl chloride701-99-52-phenoxyacetyl chloridePhenyloxyacetyl chlorideAcetyl chloride, 2-phenoxy-NSC 9808EINECS 211-862-4RefChem:861526211-862-4InChI=1/C8H7ClO2/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6HAcetyl chloride, phenoxy-Phenoxyacetylchloride
Weitere Namen anzeigen
SKL1266AKOS BBS-00003927Acyl chloride kindPhenoxyacetyl chloriphenoxy-acetylchloridLABOTEST-BB LT00643586Acetylchloride,phenoxy-PhenoxyacetylChloride>
MFCD00000726NSC-9808phenoxyacetic acid chloridePhenoxyacetic acid chloride; Phenoxyacetyl chloride; Phenoxyethanoyl chloride; Phenyloxyacetyl chloridephenoxylacetylchloride2-phenoxyacetylchloridephenoxy acetyl chloridephenoxy-acetyl chloride

Datenbank-Bezeichner

CAS
701-99-5
PubChem CID
69703
DTXSID
DTXSID1061029
UNII
NS65CKB849
EC Number
211-862-4
Nikkaji
J62.847F

Eigenschaften

Berechnete Struktureigenschaften

XLogP
2,3
Polarare Oberfläche (TPSA)
26,3 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
3
Schwere Atome
11

Physikochemische Eigenschaften

Schmelzpunkt
100 · 100-100.5 °C
Siedepunkt
225 · 225-226 °C (lit.)
Dichte
1.235 g/mL · 1.235 g/mL at 25 °C (lit.)
Brechungsindex
20 · n20/D 1.534(lit.)
Flammpunkt
227 °F · 227 °F
storage temp.
Store at RT.

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

Danger

H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]

P260, P261, P264, P271, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P319, P321, P363, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 49 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Peroxide Forming Chemical · 3 Einträge

Phenoxyacetyl chloride

D: Other compounds that may form peroxides

Kelly

Hazard Classes and CategoriesSkin Corr. 1B (100%)

Sicherheitsdaten

F
10-19
wgk
3
tsca
TSCA listed
ridadr
UN 3265 8/PG 2
hs_code
29189090
risk_code
14-34-36/37

Chemie und Industrie

Verwendung und Herstellung

General Manufacturing InformationAcetyl chloride, 2-phenoxy-: ACTIVE
Anwendungen · 1 Eintrag

VerwendenAcylation 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.

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