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Ethyl 3-oxopentanoate

Names

[ CAS No. ]:
4949-44-4

[ Name ]:
Ethyl 3-oxopentanoate

[Synonym ]:
EINECS 225-593-5
3-Oxovaleric Acid Ethyl Ester
MFCD00009317
Propionylacetic Acid Ethyl Ester
Ethyl propionylacetate
Ethyl α-methylacetylacetate
3-Ketovaleric Acid Ethyl Ester
Ethyl 3-oxopentanoate
Ethyl 3-oxo-n-valerate
Pentanoic acid, 3-oxo-, ethyl ester
Ethyl 3-oxovalerate

Biological Activity

[Description]:

Ethyl propanoylacetate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
193.0±8.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H12O3

[ Molecular Weight ]:
144.168

[ Flash Point ]:
77.8±0.0 °C

[ Exact Mass ]:
144.078644

[ PSA ]:
43.37000

[ LogP ]:
1.25

[ Vapour Pressure ]:
0.5±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.416

[ Storage condition ]:
Refrigerator

[ Stability ]:
Stable. Combustible. Incompatible with strong oxidizing agents.

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29183000

Precursor & DownStream

Customs

[ HS Code ]: 2918300090

[ Summary ]:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Etodolic acid and related compounds. Chemistry and antiinflammatory actions of some potent di- and trisubstituted 1, 3, 4, 9-tetrahydropyrano[3, 4-b]indole-1-acetic acids.

J. Med. Chem. 19(3) , 391-5, (1976)

A series of 37 1-ethyl- and 1-n-propyl-1, 3, 4, 9-tetrahydropyrano[3, 4-b]indole-1-acetic acids bearing one, or two, substituents on the benzene ring has been synthesized via the acid-catalyzed conden...

A simple and efficient synthesis of 2-alkylazulenes. Iwama N, et al.

Tetrahedron Lett. 45(50) , 9211-13, (2004)


More Articles


Related Compounds

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