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2-(4-Iodophenoxy)acetic acid

Names

[ CAS No. ]:
1878-94-0

[ Name ]:
2-(4-Iodophenoxy)acetic acid

[Synonym ]:
Acetic acid, (4-iodophenoxy)-
para-iodophenoxyacetic acid
(4-iodo-phenoxy)-acetic acid
O-(4-Jod-phenyl)-glykolsaeure
2-(4-Iodophenoxy)acetic acid
MFCD00014359
P-Iodophenoxyacetic acid
(4-Jod-phenoxy)-essigsaeure
(4-Iodophenoxy)acetic acid
Acetic acid, 2-(4-iodophenoxy)-
4-Iodophenoxyacetic Acid
EINECS 217-531-0

Chemical & Physical Properties

[ Density]:
1.9±0.1 g/cm3

[ Boiling Point ]:
358.5±22.0 °C at 760 mmHg

[ Melting Point ]:
154-157 °C(lit.)

[ Molecular Formula ]:
C8H7IO3

[ Molecular Weight ]:
278.044

[ Flash Point ]:
170.6±22.3 °C

[ Exact Mass ]:
277.943970

[ PSA ]:
46.53000

[ LogP ]:
2.60

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.628

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S24/25

[ 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

IBS-catalyzed regioselective oxidation of phenols to 1,2-quinones with Oxone®.

Molecules 17(7) , 8604-16, (2012)

We have developed the first example of hypervalent iodine(V)-catalyzed regioselective oxidation of phenols to o-quinones. Various phenols could be oxidized to the corresponding o-quinones in good to e...

Catalytic hypervalent iodine oxidation using 4-iodophenoxyacetic acid and Oxone: oxidation of p-alkoxyphenols to p-benzoquinones. Yakura T, et al.

Chem. Pharm. Bull. 57(3) , 252-256, (2009)

Prediction of acidity constant for substituted acetic acids in water using artificial neural networks. Habibi-Yangjeh A and Danandeh-Jenagharad M.

Indian J. Chem. B 46(3) , 478, (2007)


More Articles


Related Compounds

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