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2-methyl-2-[3-(trifluoromethyl)phenoxy]propanoyl chloride is a complex organic chemical compound with the molecular formula C11H10ClF3O3. It is a colorless to pale yellow liquid with a molecular weight of 287.65 g/mol. 2-methyl-2-[3-(trifluoromethyl)phenoxy]propanoyl chloride is characterized by the presence of a trifluoromethyl group (-CF3) attached to a phenyl ring, which is connected to a propanoyl chloride moiety through an ether linkage. The propanoyl chloride group is a derivative of propionic acid, where the hydroxyl group is replaced by a chlorine atom, making it highly reactive. This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drug compounds. Due to its reactivity, it is important to handle 2-methyl-2-[3-(trifluoromethyl)phenoxy]propanoyl chloride with care, typically under controlled conditions and using appropriate safety measures.

4878-30-2

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4878-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4878-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4878-30:
(6*4)+(5*8)+(4*7)+(3*8)+(2*3)+(1*0)=122
122 % 10 = 2
So 4878-30-2 is a valid CAS Registry Number.

4878-30-2Downstream Products

4878-30-2Relevant academic research and scientific papers

Pd(II)-catalyzed ortho - Or meta-C-H olefination of phenol derivatives

Dai, Hui-Xiong,Li, Gang,Zhang, Xing-Guo,Stepan, Antonia F.,Yu, Jin-Quan

supporting information, p. 7567 - 7571 (2013/06/27)

A combination of weakly coordinating auxiliaries and ligand acceleration allows for the development of both ortho- and meta-selective C-H olefination of phenol derivatives. These reactions demonstrate the feasibility of directing C-H functionalizations when functional groups are distal to target C-H bonds. The meta-C-H functionalization of electron-rich phenol derivatives is unprecedented and orthogonal to previous electrophilic substitution of phenols in terms of regioselectivity. These methods are also applied to functionalize α-phenoxyacetic acids, a fibrate class of drug scaffolds.

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