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4-acetylphenoxyacetic acid

Names

[ CAS No. ]:
1878-81-5

[ Name ]:
4-acetylphenoxyacetic acid

[Synonym ]:
(p-Acetylphenoxy)acetic acid
4-carboxymethoxy-acetophenone
EINECS 217-524-2
4-Acetylphenoxyacetic acid
(4-Acetylphenoxy)acetic Acid
MFCD00014363
2-(4-acetylphenoxy) acetic acid
2-(p-acetylphenoxy)acetic acid
Acetic acid,(4-acetylphenoxy)
(4-Acetylphenyloxy)acetic acid

Chemical & Physical Properties

[ Density]:
1.243g/cm3

[ Boiling Point ]:
380.5ºC at 760mmHg

[ Melting Point ]:
175-177 °C (dec.)(lit.)

[ Molecular Formula ]:
C10H10O4

[ Molecular Weight ]:
194.18400

[ Exact Mass ]:
194.05800

[ PSA ]:
63.60000

[ LogP ]:
1.35260

[ Vapour Pressure ]:
1.81E-06mmHg at 25°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918990090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2918990090

[ Summary ]:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Aerobic catabolism of phenylacetic acid in Pseudomonas putida U: biochemical characterization of a specific phenylacetic acid transport system and formal demonstration that phenylacetyl-coenzyme A is a catabolic intermediate.

J. Bacteriol. 176(24) , 7667-76, (1994)

The phenylacetic acid transport system (PATS) of Pseudomonas putida U was studied after this bacterium was cultured in a chemically defined medium containing phenylacetic acid (PA) as the sole carbon ...

Design of new potent hypolipidemic agents with the synergistic structural properties of α-asarone and fibrates. Zuniga C, et al.

Drug Dev. Res. 64(1) , 28-40, (2005)

Photocyclization reactions. Part 1. Synthesis of dihydrobenzofuranols using photocyclization of 2-alkoxybenzaldehydes, 2'-alkoxyacetophenones, 2-formylphenoxyacetic acids and 2-acetylphenoxyacetic acids Horaguchi T, et al.

J. Heterocycl. Chem. 28(5) , 1261-1272, (1991)


More Articles


Related Compounds