2-Iodophenylacetic acid structure
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Common Name | 2-Iodophenylacetic acid | ||
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CAS Number | 18698-96-9 | Molecular Weight | 262.044 | |
Density | 1.9±0.1 g/cm3 | Boiling Point | 344.5±17.0 °C at 760 mmHg | |
Molecular Formula | C8H7IO2 | Melting Point | 116-119ºC | |
MSDS | Chinese USA | Flash Point | 162.1±20.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 2-(2-iodophenyl)acetic acid |
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Synonym | More Synonyms |
Density | 1.9±0.1 g/cm3 |
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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 |
Symbol |
GHS07 |
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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 |
Precursor 9 | |
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DownStream 8 | |
HS Code | 2916399090 |
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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% |
Synthesis and 1 Receptor Binding of Halogenated N,N'-Diphenethylethylenediamines.
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... |
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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)
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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)
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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 |