1,1,1-Trifluoro-2-iodoethane

Synonym: 2,2,2-Trifluoroethyl iodide, 2-Iodo-1,1,1-trifluoroethane
Molecular Formula: CF3CH2I
Molecular Weight: 209.94
CAS Number: 353-83-3
MDL number: MFCD00001082
EC Number: 206-541-0
Note: Prices are for comparison only. Contact Sales for current pricing.
Purity: 99 %
Packing size: 5 G  
Form: liquid  
20.23 EUR
Purity: 99 %
Packing size: 25 G  
Form: liquid  
63.98 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P305 + P351 + P338
P261
P271
P302 + P352

Pictograms

 Product Description

1,1,1-Trifluoro-2-Iodoethane is a halogenated ethane derivative featuring both fluorine and iodine substitutions. It is used in the synthesis of various organic compounds due to its unique reactivity profile. This compound is particularly valued in the production of specialty chemicals, where its fluoroiodo motif can lead to the creation of molecules with enhanced properties, such as improved solubility or reactivity.

 

Application:

Applied in the synthesis of specialty chemicals, where its fluoroiodo functionality offers unique opportunities for the development of new materials and intermediates with tailored properties. Its use spans across industries, including pharmaceuticals, agrochemicals, and materials science, highlighting its versatility in chemical synthesis.

 

 

Articles:

- Palladium-Catalyzed Trifluoroethylation of Terminal Alkynes with 1,1,1-Trifluoro-2-iodoethane

Publication Date: February 1, 2013

Yi-Si Feng, Chuan-Qi Xie, Wen-Long Qiao and Hua-Jian Xu

-https://doi.org/10.1021/ol400099h

 

-Nickel-Catalyzed Direct Trifluoroethylation of Aryl Iodides with 1,1,1-Trifluoro-2-Iodoethane via Reductive Coupling

Publication Date: 24 September 2020

Han Li, Jie Sheng, Guang-Xu Liao, Bing-Bing Wu, Hui-Qi Ni, Yan Li, Xi-Sheng Wang

-https://doi.org/10.1002/adsc.202000985

 

-Visible-Light-Induced Photocatalysis of 1,1,1-Trifluoro-2-iodoethane with Alkylalkenes and Silyl Enol Ethers

Publication Date: 16 September 2015 (online)

Meiwei Huang, Lun Li, Zhi-Gang Zhao, Qing-Yun Chen, Yong Guo

-http://dx.doi.org/10.1055/s-0035-1560260