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2-[(2-chlorophenyl)methyl]succinic acid dimethyl ester is a chemical compound characterized by the molecular formula C13H15ClO4. It is a dimethyl ester derivative of succinic acid, featuring a chlorine-substituted phenylmethyl group. 2-[(2-chlorophenyl)methyl]succinic acid dimethyl ester is recognized for its role as an intermediate in organic synthesis, particularly in the preparation of other chemicals and pharmaceuticals.

1292292-16-0

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1292292-16-0 Usage

Uses

Used in Research and Academic Settings:
2-[(2-chlorophenyl)methyl]succinic acid dimethyl ester is utilized as a starting material for the synthesis of various chemicals and pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new compounds with potential applications in medicine and other industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[(2-chlorophenyl)methyl]succinic acid dimethyl ester is used as an intermediate for the production of specific drugs. Its chemical properties allow for the creation of molecules with therapeutic potential, contributing to the advancement of medicinal chemistry.
Used in Chemical Synthesis:
2-[(2-chlorophenyl)methyl]succinic acid dimethyl ester is employed as a key intermediate in the synthesis of specialty chemicals. Its versatility in reactions enables the production of a range of compounds with diverse applications, from industrial processes to consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 1292292-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,2,9 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1292292-16:
(9*1)+(8*2)+(7*9)+(6*2)+(5*2)+(4*9)+(3*2)+(2*1)+(1*6)=160
160 % 10 = 0
So 1292292-16-0 is a valid CAS Registry Number.

1292292-16-0Downstream Products

1292292-16-0Relevant academic research and scientific papers

Photocatalytic Radical Alkylation of Electrophilic Olefins by Benzylic and Alkylic Zinc-Sulfinates

Gualandi, Andrea,Mazzarella, Daniele,Ortega-Martínez, Aitor,Mengozzi, Luca,Calcinelli, Fabio,Matteucci, Elia,Monti, Filippo,Armaroli, Nicola,Sambri, Letizia,Cozzi, Pier Giorgio

, p. 5357 - 5362 (2017/08/17)

Alkyl radicals are obtained by photocatalytic oxidation of readily prepared or commercially available zinc sulfinates. The convenient benzylation and alkylation of a variety of electron-poor olefins triggered by the iridium(III) complex 6 Ir[dF(CF3)ppy]2(dtbbpy)PF6 as photocatalyst is described. Moreover, it is shown that zinc sulfinates can be used for facile nonradical sulfonylation reactions with highly electrophilic Michael acceptors.

Benzyl radical addition reaction through the homolytic cleavage of a benzylic C-H bond

Ueda, Masafumi,Kondoh, Eiko,Ito, Yuta,Shono, Hiroko,Kakiuchi, Maiko,Ichii, Yuki,Kimura, Takahiro,Miyoshi, Tetsuya,Naito, Takeaki,Miyata, Okiko

supporting information; experimental part, p. 2062 - 2064 (2011/05/08)

Direct generation of a benzyl radical by C-H bond activation of toluenes and the addition reaction of the resulting radical to an electron deficient olefin were developed. The reaction of dimethyl fumarate with toluene in the presence of Et3B as a radical initiator at reflux afforded 2-benzylsuccinic acid dimethyl ester in good yield.

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