Ethyl-3-oxohexanoat
CAS-Nr.
3249-68-1
Bezeichnung:
Ethyl-3-oxohexanoat
Englisch Name:
Ethyl butyrylacetate
Synonyma:
MRIO-001;FEMA 3683;AKOS 220-93;Butyrylacetate;Ethyl 3-oxohexano;Ethyl butyroacetate;Ethy Butyrylacetate;ETHYL BUTYRYLACETATE;ETHYL B-KETOCAPROATE;ETHYL 3-OXOHEXANOATE
CBNumber:
CB1748275
Summenformel:
C8H14O3
Molgewicht:
158.2
MOL-Datei:
3249-68-1.mol
Ethyl-3-oxohexanoat Eigenschaften
Schmelzpunkt:
-44°C
Siedepunkt:
104 °C22 mm Hg(lit.)
Dichte
0.989 g/mL at 25 °C(lit.)
FEMA
3683 | ETHYL 3-OXOHEXANOATE
Brechungsindex
n 20/D 1.427(lit.)
Flammpunkt:
173 °F
storage temp.
Sealed in dry,Room Temperature
L?slichkeit
soluble in Chloroform, Dichloromethane, Ethyl Acetate, Methanol
pka
10.69±0.46(Predicted)
Aggregatzustand
Liquid
Farbe
Clear colorless
Geruch (Odor)
at 100.00 %. sweet green sweaty fruity berry
Geruchsart
green
Wasserl?slichkeit
IMMISCIBLE
JECFA Number
602
BRN
507689
Stabilit?t:
Stable. Incompatible with strong oxidizing agents.
InChIKey
KQWWVLVLVYYYDT-UHFFFAOYSA-N
LogP
1.78
CAS Datenbank
3249-68-1(CAS DataBase Reference)
NIST chemische Informationen
Hexanoic acid, 3-oxo-, ethyl ester(3249-68-1)
Sicherheit
Risiko- und Sicherheitserkl?rung
Gefahreninformationscode (GHS)
S-S?tze:
24/25
RIDADR
NA 1993 / PGIII
WGK Germany
3
RTECS-Nr.
MO8420500
HS Code
29183000
Bildanzeige (GHS)
Alarmwort
Warnung
Gefahrenhinweise
Code
Gefahrenhinweise
Gefahrenklasse
Abteilung
Alarmwort
Symbol
P-Code
H227
Combustible liquid
Flammable liquids
Category 4
Warnung
P210, P280, P370+P378, P403+P235,P501
H301
Giftig bei Verschlucken.
Akute Toxizit?t oral
Kategorie 3
Achtung
src="/GHS06.jpg" width="20" height="20" />
P264, P270, P301+P310, P321, P330,P405, P501
Sicherheit
P403+P235
An einem gut belüfteten Ort aufbewahren. Kühl halten.
P405
Unter Verschluss aufbewahren.
Ethyl-3-oxohexanoat Chemische Eigenschaften,Einsatz,Produktion Methoden
S-S?tze Betriebsanweisung:
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
colourless liquid
Verwenden
Ethyl Butyrylacetate is used in the synthesis of pharmaceutical agents such as the anti-HIV agent (+/-)-Calanolide A.Also used in the synthesis of potent and selective polymerase inhibitors.
Allgemeine Beschreibung
Ethyl 3-oxohexanoate is a volatile flavor ester that is reported to occur in banana fruit. It can undergo bioreduction to form ethyl (
R )-3-hydroxyhexanoate, another key food flavoring agent.
Ethyl-3-oxohexanoat Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Ethyl-3-oxohexanoat Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 278)Lieferanten
Americas 1
Belgium 3
China 203
Europe 2
France 1
Germany 9
India 3
Italy 1
Japan 4
Slovakia 1
Switzerland 2
Ukraine 1
United Kingdom 7
United States 39
USA 1
Global 278
3249-68-1(Ethyl-3-oxohexanoat)Verwandte Suche:
Ethyl Butyrylacetate
Ethyl 3-Ketohexanoate
3-Ketohexanoic Acid Ethyl Ester
3-Oxohexanoic Acid Ethyl Ester
3-oxo-hexanoicaciethylester
ETHYL BUTYRYLACETATE FOR SYNTHESIS
Ethyl 3-oxohexano
Ethyl 3-oxocaproate, Ethyl butyrylacetate, Ethyl butanoylacetate
Butyrylacetate
Ethyl 3-oxohexanoate 98%
Ethy Butyrylacetate
Ethyl alpha-butyrylacetate
Ethyl butyroacetate
3-KETOHEXANOIC ACID ETHYL ESTER
3-KETO-N-HEXANOIC ACID ETHYL ESTER
3-OXOHEXANOIC ACID ETHYL ESTER
AKOS 220-93
BUTYRYLACETIC ACID ETHYL ESTER
FEMA 3683
ETHYL BUTYROYL ACETATE
ETHYL BUTYRYLACETATE
ETHYL B-KETOCAPROATE
Ethyl beta-ketohexanoate
ETHYL 3-OXOHEXANOATE
ETHYL 3-KETOHEXANOATE
Butyrylacetic acid ethyl ester~Ethyl 3-oxohexanoate~3-Oxohexanoic acid ethyl ester
ETHYL 3-OXOHEXANOATE 98+%
ERHYL BUTYRYLACETATE
Ethylbutyrylacetate,98%
Ehtyl butyryl acetate
Hexanoic acid, 3-oxo-, ethyl ester
3-Ketocaproic acid ethyl ester
Ethyl 3-oxohexanoate,Ethyl butyrylacetate
3-ethyl-4-oxohexanoate
Ethyl butyrylacetate, 98% 25GR
MRIO-001
Ethyl3-Oxohexanoate>
Ethyl butyrylacetate USP/EP/BP
Propylthiouracil Impurity 11
Mirogabalin Impurity 63
3249-68-1
CH3CH2CH2COCH2COOC2H5
Building Blocks
Carbonyl Compounds
C8 to C9
ACETATE
Esters
Organic Building Blocks
Pharmaceutical Intermediates
BUILDING BLOCKS
C8 to C9
Carbonyl Compounds
Chemical Synthesis
Esters
Organic Building Blocks