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Ethyl-3-iodobenzoate

Names

[ CAS No. ]:
58313-23-8

[ Name ]:
Ethyl-3-iodobenzoate

[Synonym ]:
3-ethoxycarbonyl-1-iodobenzene
ETHYL-3-IODOBENZOATE
ethyl 3-iodoethylbenzoate
3-EtO2C-C6H4-I
Benzoic acid, 3-iodo-, ethyl ester
3-Iodobenzoic Acid Ethyl Ester
ETHYL M-IODOBENZOATE
Ethyl 3-iodobenzoate
MFCD00044769
3-iodobenzoic acid methyl ester
Ethyl 3-iodophenylbenzoate

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
299.3±23.0 °C at 760 mmHg

[ Molecular Formula ]:
C9H9IO2

[ Molecular Weight ]:
276.071

[ Flash Point ]:
134.8±22.6 °C

[ Exact Mass ]:
275.964722

[ PSA ]:
26.30000

[ LogP ]:
3.84

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

[ Index of Refraction ]:
1.585

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

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

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2916399090

Synthetic Route

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

Acidic heterocycles as novel hydrophilic pharmacophore of androgen receptor ligands with a carborane core structure.

Bioorg. Med. Chem. 17(1) , 344-50, (2009)

A novel series of androgen receptor (AR) ligands bearing an acidic heterocycle with hydrogen-bonding ability as the terminal polar group was developed. Since most non-steroidal AR ligands so far known...

Ni (II)-catalyzed cross-coupling between polyfunctional arylzinc derivatives and primary alkyl iodides. Giovannini R and Knochel P.

J. Am. Chem. Soc. 120(43) , 11186-11187, (1998)

Copper catalyzed conjugate addition of highly functionalized arylmagnesium compounds to enones. Varchi G, et al.

Tetrahedron 56(18) , 2727-2731, (2000)


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Related Compounds

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