1077-01-6 Usage
General Description
3-(Trifluoromethoxy)fluorobenzene is a specialized chemical compound, also known as C7H4F4O. It contains a benzene ring, which is attached to a trifluoromethoxy group and a fluorine atom. 3-(Trifluoromethoxy)fluorobenzene falls under the category of organofluorines, which are characterized by their carbon–fluorine bonds, and more specifically, it's a type of aryl halide, which are known for their use in pharmaceuticals and agrochemicals. Its molecular weight is approximately 186.1 g/mol. Its specific properties, such as boiling, melting point and density, mainly depend on conditions like temperature and pressure. Moreover, safety measures should be undertaken while handling due to it potentially being hazardous.
Check Digit Verification of cas no
The CAS Registry Mumber 1077-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1077-01:
(6*1)+(5*0)+(4*7)+(3*7)+(2*0)+(1*1)=56
56 % 10 = 6
So 1077-01-6 is a valid CAS Registry Number.
InChI:InChI:1S/C7H4F4O/c8-5-2-1-3-6(4-5)12-7(9,10)11/h1-4H
1077-01-6Relevant articles and documents
Mathey,Bensoam
, p. 2253 (1973)
Photocatalytic trifluoromethoxylation of arenes and heteroarenes in continuous-flow
Cendón, Borja,Gulías, Moisés,Ho, Michelle,No?l, Timothy,Nyuchev, Alexander V.,Sambiagio, Carlo,Struijs, Job J. C.,Wan, Ting,Wang, Ying
supporting information, p. 1305 - 1312 (2020/07/10)
The first example of photocatalytic trifluoromethoxylation of arenes and heteroarenes under continuous-flow conditions is described. Application of continuous-flow microreactor technology allowed to reduce the residence time up to 16 times in comparison t
DIFLUOROMETHOXYLATION AND TRIFLUOROMETHOXYLATION COMPOSITIONS AND METHODS FOR SYNTHESIZING SAME
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Page/Page column 75; 79; 118-119; 120, (2019/09/18)
The present invention provides a compound having the structure (I), a processing of making the compound; and a process of using the compound as a reagent for the difluoromethoxylation and trifluoromethoxylation of arenes or heteroarenes.
