2-Fluor-1-phenylethan-1-on

2-fluoro-1-phenylethan-1-one · 2-fluoro-1-phenylethanone · Phenacyl fluoride · α-Fluoroacetophenone · O-FLUOROACETOPHENONE · LABOTEST-BB LT01148268 · alpha-Fluoroacetophenone · omega-Fluoroacetophenone

https://huagongshe.com/de/chemical/9947

Molekülstruktur von 2-Fluor-1-phenylethan-1-on

Identifikatoren & physikalische Daten

CAS No.	450-95-3
Summenformel	C8H7FO
Durchschnittliche Molmasse	138,14 g/mol
Monoisotopische Masse	138,04809306 g/mol
SMILES	O=C(CF)c1ccccc1
InChIKey	YOMBUJAFGMOIGS-UHFFFAOYSA-N
PubChem CID	9947
EC No.	207-190-6
DTXSID	DTXSID90196360
Lokaler Name	2-Fluor-1-phenylethan-1-on

Chemische & physikalische Eigenschaften

XLogP	2,1
Polarare Oberfläche (TPSA)	17,1
H-Brücken-Donoren	0
H-Brücken-Akzeptoren	2
Frei drehbare Bindungen	2
Schwere Atome	10
Formalladung	0
Komplexität	116
SpringerMaterials Properties	19F nuclear magnetic resonance spectrum
Schmelzpunkt	26-27
Siedepunkt	187-189 °C(lit.)
Dichte	1.137 g/mL at 20 °C(lit.)
Brechungsindex	n20/D 1.507(lit.)
Flammpunkt	143 °F
Lagerbedingungen	Storage temp. 2-8°C
Aggregatzustand	fused solid
Farbe	Off-white
InChI	InChI=1S/C8H7FO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2
InChIKey	YOMBUJAFGMOIGS-UHFFFAOYSA-N
SMILES	C(=O)(C1=CC=CC=C1)CF
CAS Datenbank	450-95-3(CAS DataBase Reference)

Sicherheit & Vorschriften

GHS-Einstufung	DangerH227 (50%): Combustible liquid [Warning Flammable liquids]P210, P260, P261, P264, P271, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P319, P321, P363, P370+P378, P403, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and Categories	Flam. Liq. 4 (50%)
Wassergefährdungsklasse (WGK)	3
Zollcode	29147000
R-Sätze (R)	36/37/38
Gefahrensymbole	Xi,F
Sicherheitshinweise (S)	26-36

Anwendungen & Verwendung

Verwenden

2-Fluoroacetophenone is used in method for synthesizing -Fluorinated Ketone by hydrazonation of fatty chain monoketone.