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About This Item
线性分子式:
IC6H4CH2CO2H
CAS号:
分子量:
262.04
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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品質等級
化驗
97%
mp
116-119 °C (lit.)
官能基
carboxylic acid
iodo
SMILES 字串
OC(=O)Cc1ccccc1I
InChI
1S/C8H7IO2/c9-7-4-2-1-3-6(7)5-8(10)11/h1-4H,5H2,(H,10,11)
InChI 密鑰
IUHXGZHKSYYDIL-UHFFFAOYSA-N
一般說明
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.
應用
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
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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Photochemical synthesis of aromatic chloro compounds from aromatic iodo compounds.
The Journal of Organic Chemistry, 35(2), 528-529 (1970)
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.
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European Journal of Organic Chemistry, 5927-5940 (2009)
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Taylor SR, et al.
Tetrahedron, 63(45), 10889-10895 (2007)
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Medicinal chemistry, 1(102) (2011-12-25)
Eight halogenated
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