349-59-7 Usage
Description
3,5-BIS(TRIFLUOROMETHYL)STYRENE is an organic compound that features a styrene structure with two trifluoromethyl groups attached to the 3 and 5 positions of the benzene ring. 3,5-BIS(TRIFLUOROMETHYL)STYRENE is known for its unique chemical properties and reactivity, making it a valuable intermediate in the synthesis of various chemicals and materials.
Uses
Used in Chemical Synthesis:
3,5-BIS(TRIFLUOROMETHYL)STYRENE is used as a chemical intermediate for the production of other chemicals, such as 1-(3, 5-bis-Trifluoromethyl-phenyl)-ethane-1, 2-diol. Its unique structure and reactivity make it a versatile building block in the synthesis of various compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-BIS(TRIFLUOROMETHYL)STYRENE can be used as a starting material for the development of new drugs with specific therapeutic properties. Its unique chemical structure may contribute to the design of novel molecules with improved pharmacological profiles.
Used in Polymer Industry:
3,5-BIS(TRIFLUOROMETHYL)STYRENE can also be utilized in the polymer industry as a monomer for the synthesis of polymers with specific properties, such as enhanced thermal stability, chemical resistance, or mechanical strength. These polymers can find applications in various sectors, including automotive, electronics, and aerospace.
Used in Agrochemical Industry:
In the agrochemical industry, 3,5-BIS(TRIFLUOROMETHYL)STYRENE may be employed as a precursor for the development of new pesticides or other agrochemical products. Its unique chemical structure could potentially lead to the creation of more effective and environmentally friendly solutions for pest control and crop protection.
Overall, 3,5-BIS(TRIFLUOROMETHYL)STYRENE is a versatile compound with a wide range of potential applications across various industries, including chemical synthesis, pharmaceuticals, polymers, and agrochemicals. Its unique structure and reactivity make it a valuable intermediate for the development of new products and materials with improved properties and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 349-59-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 349-59:
(5*3)+(4*4)+(3*9)+(2*5)+(1*9)=77
77 % 10 = 7
So 349-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H6F6/c1-2-6-3-7(9(11,12)13)5-8(4-6)10(14,15)16/h2-5H,1H2
349-59-7Relevant articles and documents
In-situ facile synthesis novel N-doped thin graphene layer encapsulated Pd@N/C catalyst for semi-hydrogenation of alkynes
Lin, Shanshan,Liu, Jianguo,Ma, Longlong,Sun, Jiangming
, (2021/12/03)
Transition metal-catalyzed semi-hydrogenation of alkynes has become one of the most popular methods for alkene synthesis. Specifically, the noble metal Pd, Rh, and Ru-based heterogeneous catalysts have been widely studied and utilized in both academia and industry. But the supported noble metal catalysts are generally suffering from leaching or aggregation during harsh reaction conditions, which resulting low catalytic reactivity and stability. Herein, we reported the facile synthesis of nitrogen doped graphene encapsulated Pd catalyst and its application in the chemo-selective semi-hydrogenation of alkynes. The graphene layer served as “bulletproof” over the active Pd Nano metal species, which was confirmed by X-ray and TEM analysis, enhanced the catalytic stability during the reaction conditions. The optimized prepared Pd@N/C catalyst showed excellent efficiency in semi-hydrogenation of phenylacetylene and other types of alkynes with un-functionalized or functionalized substituents, including the hydrogenation sensitive functional groups (NO2, ester, and halogen).
Process for making hydroisoindoline tachykinin receptor antagonists
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Page/Page column 14; 15, (2008/06/13)
The present invention is directed to a process for preparing certain hydroisoindoline compounds which are useful as neurokinin-1 (NK-1) receptor antagonists, and inhibitors of tachykinin and in particular substance P. The compounds are useful in the treatment of certain disorders, including emesis, urinary incontinence, depression, and anxiety.
Crystallization-induced diastereoselection: Asymmetric synthesis of substance P inhibitors
Pye, Philip J.,Rossen, Kai,Weissman, Steven A.,Maliakal, Ashok,Reamer, Robert A.,Ball, Richard,Tsou, Nancy N.,Volante,Reider, Paul J.
, p. 1372 - 1376 (2007/10/03)
A novel three-component condensation followed by a crystallization-induced asymmetric transformation is used to build this key substance P inhibitor intermediate in a short synthetic sequence.