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Merck
CN

531472

2-碘苯乙酸

97%

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线性分子式:
IC6H4CH2CO2H
化学文摘社编号:
分子量:
262.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

2-碘苯乙酸, 97%

InChI

1S/C8H7IO2/c9-7-4-2-1-3-6(7)5-8(10)11/h1-4H,5H2,(H,10,11)

SMILES string

OC(=O)Cc1ccccc1I

InChI key

IUHXGZHKSYYDIL-UHFFFAOYSA-N

assay

97%

mp

116-119 °C (lit.)

functional group

carboxylic acid
iodo

Quality Level

Application

2-Iodophenylacetic acid may be used in the preparation of:
  • 2-iodophenylacetyl chloride
  • 3,4-dimethoxyphenyl 2-iodophenylacetate
  • N-{2-[2-(2-iodophenyl)-acetylamino]-ethyl}-2-(3,4- dichlorophenyl)-acetamide

General description

2-Iodophenylacetic acid is a substituted acetic acid that can be prepared from 2-iodobenzyl cyanide. It undergoes palladium-catalyzed reaction with allenes to form 1,3-butadienes. 2-Iodophenylacetic acid also undergoes photolysis in carbon tetrachloride to form the corresponding chloro compound.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis of benzo[c]chromen-6-ones via novel cyclic aryl?Pd (II)?ester enolate intermediates.
Taylor SR, et al.
Tetrahedron, 63(45), 10889-10895 (2007)
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 Journal of Organic Chemistry, 5927-5940 (2009)
Photochemical synthesis of aromatic chloro compounds from aromatic iodo compounds.
The Journal of Organic Chemistry, 35(2), 528-529 (1970)
Regioselective Synthesis of Isoquino [1,2-b][3] benzazepines (Homoprotoberberines) through 11-Membered-Ring Stilbene Lactams Obtained by Radical Macrocyclization.
Rodriguez G, et al.
The Journal of Organic Chemistry, 64(13), 4830-4833 (1999)
Jonathan M Fitzsimmons et al.
Medicinal chemistry, 1(102) (2011-12-25)
Eight halogenated

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