所有图片(1)
About This Item
线性分子式:
(CH3)2C6H3I
CAS号:
分子量:
232.06
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
99%
表单
liquid
折射率
n20/D 1.603 (lit.)
沸点
106-108 °C/13 mmHg (lit.)
密度
1.633 g/mL at 25 °C (lit.)
SMILES字符串
Cc1ccc(I)cc1C
InChI
1S/C8H9I/c1-6-3-4-8(9)5-7(6)2/h3-5H,1-2H3
InChI key
CSFRCLYFVINMBZ-UHFFFAOYSA-N
一般描述
1-Iodo-3,4-dimethylbenzene (4-iodo-o-xylene, 3,4-dimethyliodobenzene) is an aryl halide. Its synthesis, NMR and IR spectra has been reported. Its nitration reaction and copper catalyzed trifluoromethylation reaction has been studied.
应用
1-Iodo-3,4-dimethylbenzene (4-iodo-o-xylene, 3,4-dimethyliodobenzene) may be used in the synthesis of the following:
- 3-arylacrylamide
- 3,3-diaryl substituted acrylamide
- 3-arylpropylamine
- di-tert-butyl 1-(3,4-dimethylphenyl)hydrazine-1,2-dicarboxylate
- 2,3,7,8-tetramethyldibenzofuran
- N-(3-(3,4-Dimethylphenyl)-2-phthalimidopropionyl)-2-methylthioaniline
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
Synthesis of 3-arylpropylamine derivatives from aryl halides using Heck reaction.
Baek GH, et al.
Bull. Korean Chem. Soc., 20, 232-236 (1999)
Efficient and direct iodination of alkyl benzenes using polymer/HIO4 and I2 under mild condition.
Pourali AR, et al.
Bulletin of the Chemical Society of Ethiopia, 28(2), 305-308 (2014)
Synthesis of 2, 3, 7, 8-tetramethyldibenzofuran.
Mazere IV, et al.
Chemistry of Heterocyclic Compounds, 8(12), 1446-1448 (1972)
Towards a practical and efficient copper-catalyzed trifluoromethylation of aryl halides.
Schareina T, et al.
Topics in Catalysis, 55(7-10), 426-431 (2012)
Dmitry Shabashov et al.
Journal of the American Chemical Society, 132(11), 3965-3972 (2010-02-24)
We have developed a method for auxiliary-directed, palladium-catalyzed beta-arylation and alkylation of sp(3) and sp(2) C-H bonds in carboxylic acid derivatives. The method employs a carboxylic acid 2-methylthioaniline- or 8-aminoquinoline amide substrate, aryl or alkyl iodide coupling partner, palladium acetate
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