2-Iodophenylacetic acid
Suppliers
Names
[ CAS No. ]:
18698-96-9
[ Name ]:
2-Iodophenylacetic acid
[Synonym ]:
MFCD00046546
2-(2-Iodophenyl)acetic acid
2-Iodophenylacetic acid
2-Iodobenzeneacetic acid
(2-Iodophenyl)acetic acid
Benzeneacetic acid, 2-iodo-
ortho-Iodophenylacetic acid
o-iodophenylacetic acid
2-Iodophenyl acetic acid
Chemical & Physical Properties
[ Density]:
1.9±0.1 g/cm3
[ Boiling Point ]:
344.5±17.0 °C at 760 mmHg
[ Melting Point ]:
116-119ºC
[ Molecular Formula ]:
C8H7IO2
[ Molecular Weight ]:
262.044
[ Flash Point ]:
162.1±20.9 °C
[ Exact Mass ]:
261.949066
[ PSA ]:
37.30000
[ LogP ]:
2.54
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.643
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
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2916399090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2916399090
[ Summary ]:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Med. Chem. (Los Angeles) 1(102) , (2011)
Eight halogenated N,N'-diphenethylethylenediamines were synthesized, characterized and evaluated for 1 receptor binding affinity in vitro. Measurements of lipophilicity also were obtained. The substit...
Regioselective Synthesis of Isoquino [1,2-b][3] benzazepines (Homoprotoberberines) through 11-Membered-Ring Stilbene Lactams Obtained by Radical Macrocyclization. Rodríguez G, et al.J. Org. Chem. 64(13) , 4830-4833, (1999)
Pd‐Catalyzed Reactions of Allenylphosphonates and Related Allenes with Functionalized 2‐Iodophenols, 2‐Iodobenzoic Acid, and 2‐Iodobenzyl Alcohol Leading to Functionalized Benzofurans, Isocoumarins, and Benzopyrans. Pavan MP, et al.
European J. Org. Chem. , 5927-5940, (2009)