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Methyl 4-Hydroxyphenylacetate

Names

[ CAS No. ]:
14199-15-6

[ Name ]:
Methyl 4-Hydroxyphenylacetate

[Synonym ]:
Casaron
4-Hydroxyphenylacetic Acid Methyl Ester
Dichlobenil
2,6-Dichlorobenzonitrile
Casoron G
EINECS 238-050-2
Niagara 5996
2,6-Dichlorocyanobenzene
2,6-Dichlorophenyl cyanide
Methyl 4-Hydroxyphenylacetate
NCR BG FG
Benzonitrile, 2,6-dichloro-
MFCD00002387

Biological Activity

[Description]:

Methyl 4-hydroxyphenylacetate, a natural compound, is a methyl ester resulting from the formal condensation of the carboxy group of 4-Hydroxyphenylacetic acid with methanol[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[References]

[1]. Rong-Qing Mei, et al. A new phenol derivative isolated from mangrove-derived fungus Eupenicillium sp. HJ002. Nat Prod Res. 2020 Jan 21;1-7.

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
279.2±20.0 °C at 760 mmHg

[ Melting Point ]:
55-58 °C(lit.)

[ Molecular Formula ]:
C9H10O3

[ Molecular Weight ]:
172.011

[ Flash Point ]:
126.8±16.0 °C

[ Exact Mass ]:
170.964249

[ PSA ]:
46.53000

[ LogP ]:
2.79

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.584

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:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2916399090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2918290000

[ Summary ]:
HS: 2918290000 other carboxylic acids with phenol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) VAT:17.0% MFN tariff:6.5% General tariff:30.0%

Articles

Enantioselective preparation of metoprolol and its major metabolites.

Arch. Pharm. Res. 23(3) , 226-9, (2000)

To obtain the standard compounds of metoprolol for a pharmacokinetic study, a convenient synthetic procedure to prepare enantiomers of metoprolol (3a) and its major metabolites, 2-4-(2-hydroxy-3-isopr...

A novel and other bioactive secondary metabolites from a marine fungus Penicillium oxalicum 0312F1.

Nat. Prod. Res. 27(24) , 2286-91, (2013)

A new compound 2-(4-hydroxybenzoyl) quinazolin-4(3H)-one (1) and four known compounds were isolated from a marine fungus Penicillium oxalicum 0312F1. The structure of the new compound 1 was elucidated...


More Articles


Related Compounds

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