1737-11-7 Usage
Uses
Used in Organic Synthesis:
4-(1,1,2,2-Tetrafluoroethoxy)toluene is used as a reagent in organic synthesis for its ability to facilitate chemical reactions, contributing to the formation of desired products in the synthesis process.
Used as an Intermediate in Chemical Production:
4-(1,1,2,2-Tetrafluoroethoxy)toluene serves as an intermediate in the production of other chemicals, indicating its role in the synthesis of more complex molecules or in the manufacturing of various chemical products.
Used in Various Industries as a Solvent:
4-(1,1,2,2-Tetrafluoroethoxy)toluene is commonly utilized as a solvent across different industries due to its ability to dissolve a wide range of substances, which is crucial for numerous applications and processes.
Used in the Plastics Industry:
In the plastics industry, 4-(1,1,2,2-Tetrafluoroethoxy)toluene is used as a solvent for its compatibility with plastic materials, aiding in the manufacturing and processing of plastic products.
Used in the Elastomers Industry:
Similarly, in the elastomers industry, 4-(1,1,2,2-Tetrafluoroethoxy)toluene is used as a solvent to work with elastomeric materials, which are essential in the production of various rubber-based products.
Used in the Metalworking Industry:
4-(1,1,2,2-Tetrafluoroethoxy)toluene is also used in the metalworking industry as a solvent for its compatibility with metals, playing a role in metal cleaning, degreasing, or other processes where solvents are required.
Check Digit Verification of cas no
The CAS Registry Mumber 1737-11-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1737-11:
(6*1)+(5*7)+(4*3)+(3*7)+(2*1)+(1*1)=77
77 % 10 = 7
So 1737-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8F4O/c1-6-2-4-7(5-3-6)14-9(12,13)8(10)11/h2-5,8H,1H3
1737-11-7Relevant academic research and scientific papers
Kamal, Ahmed,Pratap,Ramana, K.Venkata,Ramana,Babu, A.Hari
, p. 7353 - 7355 (2002)
A convenient and practical method for the preparation of fluoroalkyl aryl ethers via substitution of iodoalkyl fluorides is described. This method involves KF complexation of the phenol, which increases the nucleophilicity of oxygen for the formation of the ether linkage.
CONDENSATION OF 1,2-DIBROMOTETRAFLUOROETHANE WITH VARIOUS POTASSIUM THIOPHENOXIDES AND PHENOXIDES
Rico, I.,Wakselman, C.
, p. 759 - 764 (2007/10/02)
BrCF2CF2Br reacts easily with various potassium thiophenoxides and phenoxides to give respectively 2-bromo tetrafluoroethyl thioethers and ethers.The lipophilicity of C6H5SCF2CF2Br and C6H5OCF2CF2Br is measured and compared with that of the well known C6H5SCF2CF2H and C6H5OCF2CF2H.
M-phenoxybenzyl and α-cyano-M-phenoxybenzyl esters of 2-haloalkyl (oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids
-
, (2008/06/13)
The invention is m-phenoxybenzyl esters of 2-haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids which are useful insecticidal and acaricidal agents.
2-Haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)-phenylalkanoic acids
-
, (2008/06/13)
The invention is 2-haloalkyl(oxy-, thio-, sulfinyl-, or sulfonyl)phenylalkanoic acids which are useful intermediates in the preparation of insecticides of m-phenoxybenzyl and α-cyano-m-phenoxybenzyl esters.
