1813-97-4 Usage
Description
3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is an organic compound characterized by its unique molecular structure, which features a propene backbone with a trifluoromethylphenyl group attached at the 3rd position. 3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is known for its reactivity and versatility in various chemical reactions, making it a valuable intermediate in the synthesis of a wide range of products.
Uses
3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is used as a reactant for the stereoselective preparation of alkenyl nitriles via FeCl2-catalyzed oxidation. This application takes advantage of the compound's reactivity and ability to form specific stereoisomers, which are crucial in the development of pharmaceuticals and other specialty chemicals.
3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is also used as a reactant in the regioselective intermolecular allylic C-H alkylation with bis-sulfoxide/Pd(OAc)2 catalyst. This reaction allows for the selective formation of desired products with specific structural features, which can be important in the synthesis of complex organic molecules and materials.
Used in Pharmaceutical Industry:
3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity enable the development of new drugs with improved efficacy and selectivity.
Used in Chemical Industry:
In the chemical industry, 3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is used as a building block for the production of specialty chemicals, such as fragrances, dyes, and additives. Its versatility in chemical reactions allows for the creation of a diverse range of products with specific properties and applications.
Used in Material Science:
3-[(4-TRIFLUOROMETHYL)PHENYL]-1-PROPENE is utilized in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties. Its incorporation into these materials can lead to improved performance characteristics, such as enhanced stability, durability, and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 1813-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1813-97:
(6*1)+(5*8)+(4*1)+(3*3)+(2*9)+(1*7)=84
84 % 10 = 4
So 1813-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F3/c1-2-3-8-4-6-9(7-5-8)10(11,12)13/h2,4-7H,1,3H2
1813-97-4Relevant articles and documents
The Enantioselective Copolymerisation of Allylbenzene, 1-Allyl-4-(trifluoromethyl)benzene, and 1-Allyl-4-methoxybenzene with Carbon Monoxide
Di Benedetto, Silvia,Consiglio, Giambattista
, p. 2204 - 2214 (1997)
The olefins mentioned in the title were copolymerized with CO in the presence of palladium catalysts modified with dicyclohexyl {(R)-1-[(S)-2-(diphenylphosphino)ferrocenyl]ethyl}phosphine. Productivities up to 95 g/(g Pd · h) were achieved. The obtained c
Photo-Ni-Dual-Catalytic C(sp2)-C(sp3) Cross-Coupling Reactions with Mesoporous Graphitic Carbon Nitride as a Heterogeneous Organic Semiconductor Photocatalyst
Antonietti, Markus,Ghosh, Indrajit,K?nig, Burkhard,Khamrai, Jagadish,Savateev, Aleksandr
, p. 3526 - 3532 (2020/04/09)
The synergistic combination of a heterogeneous organic semiconductor mesoporous graphitic carbon nitride (mpg-CN) and a homogeneous nickel catalyst with visible-light irradiation at room temperature affords the C(sp2)-C(sp3) cross-co
Palladium-Catalyzed Oxidative Allylation of Sulfoxonium Ylides: Regioselective Synthesis of Conjugated Dienones
Li, Chunsheng,Li, Meng,Zhong, Wentao,Jin, Yangbin,Li, Jianxiao,Wu, Wanqing,Jiang, Huanfeng
supporting information, p. 872 - 875 (2019/05/16)
The first examples of palladium-catalyzed allylic C-H oxidative allylation of sulfoxonium ylides to afford the corresponding conjugated dienones with moderate to good yields have been established. The features of this novel conversion include mild reaction conditions, wide substrate scope, and excellent regioselectivity.
