141743-49-9 Usage
General Description
2,6-Difluoro-4-iodoaniline is a chemical compound that belongs to the class of aniline derivatives, specifically substituted anilines. It is a yellow to brown solid with a molecular formula C6H5F2IN. This chemical is used in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its applications include as an intermediate in the production of various organic compounds, including pharmaceuticals and dyes. It is also used as a building block in the manufacture of materials such as polymers and resins. Additionally, 2,6-Difluoro-4-iodoaniline is used in research and development to explore its potential applications in various industries. However, it is important to handle this chemical with caution and adhere to proper safety protocols, as it may present hazards if not handled and stored properly.
Check Digit Verification of cas no
The CAS Registry Mumber 141743-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,7,4 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141743-49:
(8*1)+(7*4)+(6*1)+(5*7)+(4*4)+(3*3)+(2*4)+(1*9)=119
119 % 10 = 9
So 141743-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F2IN/c7-4-1-3(9)2-5(8)6(4)10/h1-2H,10H2
141743-49-9Relevant articles and documents
Reversible Stereoselective Folding/Unfolding Fueled by the Interplay of Photoisomerism and Hydrogen Bonding
Opie, Christopher R.,Kumagai, Naoya,Shibasaki, Masakatsu
, p. 3349 - 3353 (2017)
A linear molecular architecture equipped with complementary three-fold hydrogen-bonding units embedded with a photoswitchable trans-tetrafluoroazobenzene moiety was synthesized. The transto cis photoisomerism of the azobenzene unit induced drastic changes
COMPOSITION AND METHOD FOR MANUFACTURING RESINS
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Paragraph 0182, (2021/05/07)
Certain embodiments of the invention described herein comprise a composition of matter, and method for preparing the same, which provide the benefits of pre-reaction molecular configuration favoring high liquidity properties, and post-reaction configurati
O -fluoroazobenzenes as readily synthesized photoswitches offering nearly quantitative two-way isomerization with visible light
Bleger, David,Schwarz, Jutta,Brouwer, Albert M.,Hecht, Stefan
supporting information, p. 20597 - 20600 (2013/02/22)
Azobenzene functionalized with ortho-fluorine atoms has a lower energy of the n-orbital of the Z-isomer, resulting in a separation of the E and Z isomers' n→π* absorption bands. Introducing para-substituents allows for further tuning of the absorption spe
