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1-Isopropoxy-4-(trifluoromethyl)benzene is an organic compound with the molecular formula C10H11F3O. It is a colorless liquid at room temperature and is characterized by its distinct chemical structure, which includes a benzene ring with an isopropoxy group at the 1-position and a trifluoromethyl group at the 4-position. 1-isopropoxy-4-(trifluoromethyl)benzene is known for its unique properties, such as its low reactivity and stability, which make it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its specific functional groups, it can be used in reactions involving nucleophilic substitution, electrophilic aromatic substitution, and other organic transformations. The compound's physical properties, such as its boiling point, melting point, and solubility, can be influenced by the presence of the electron-withdrawing trifluoromethyl group and the electron-donating isopropoxy group, which can affect its reactivity and applications in chemical synthesis.

618-23-5

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618-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 618-23-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 618-23:
(5*6)+(4*1)+(3*8)+(2*2)+(1*3)=65
65 % 10 = 5
So 618-23-5 is a valid CAS Registry Number.

618-23-5Downstream Products

618-23-5Relevant articles and documents

Coupling of Alternating Current to Transition-Metal Catalysis: Examples of Nickel-Catalyzed Cross-Coupling

Bortnikov, Evgeniy O.,Semenov, Sergey N.

, p. 782 - 793 (2021)

The coupling of transition-metal to photoredox catalytic cycles through single-electron transfer steps has become a powerful tool in the development of catalytic processes. In this work, we demonstrated that transition-metal catalysis can be coupled to al

A Unified and Practical Method for Carbon–Heteroatom Cross-Coupling using Nickel/Photo Dual Catalysis

Escobar, Randolph A.,Johannes, Jeffrey W.

supporting information, (2020/04/17)

While carbon–heteroatom cross-coupling reactions have been extensively studied, many methods are specific and limited to a particular set of substrates or functional groups. Reported here is a general method that allows for C?O, C?N and C?S cross-coupling reactions under one general set of conditions. We propose that an energy transfer pathway, in which an iridium photosensitizer produces an excited nickel(II) complex, is responsible for the key reductive elimination step that couples aryl bromides, iodides, and chlorides to 1° and 2° alcohols, amines, thiols, carbamates, and sulfonamides, and is amenable to scale up via a flow apparatus.

POLY-N-HETEROCYCLIC CARBENE TRANSITION METAL COMPLEXES AND N-HETEROCYCLIC CARBENE TRANSITION METAL COMPLEXES FOR CARBON-SULFUR AND CARBON-OXYGEN COUPLING REACTIONS

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Page/Page column 24-25, (2009/01/20)

Methods for carbon-sulfur (C S) or carbon-oxygen (C-O) coupling reactions are provided. The methods involve the use of a transition metal complex comprising a heterocyclic carbene ligand complexed with a transition metal. Transition metal complexes comprising a heterocyclic carbene ligand complexed with nickel are also provided. The nickel heterocylic carbene complexes may be used for C-S or C-O coupling reactions.

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