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α-Methyl-β-(p-methoxyphenyl)-propionyl chloride is a chemical compound with the molecular formula C11H13ClO2. It is a derivative of propionyl chloride, featuring a methyl group at the alpha position, a p-methoxyphenyl group at the beta position, and a chlorine atom attached to the carbonyl carbon. α-methyl-β-(p-methoxyphenyl)-propionyl chloride is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactivity and versatility. It can be used in the formation of esters, amides, and other functional groups through nucleophilic substitution reactions. The presence of the p-methoxyphenyl group provides additional opportunities for further functionalization and modification, making it a valuable building block in organic synthesis.

56935-39-8

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56935-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56935-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56935-39:
(7*5)+(6*6)+(5*9)+(4*3)+(3*5)+(2*3)+(1*9)=158
158 % 10 = 8
So 56935-39-8 is a valid CAS Registry Number.

56935-39-8Relevant academic research and scientific papers

Catalytic enantioselective desymmetrization of cyclobutane-1,3diones by carbonyl-amine condensation

Wen, Kai-Ge,Liu, Chao,Wei, Dong-Hui,Niu, Yan-Fei,Peng, Yi-Yuan,Zeng, Xing-Ping

supporting information, p. 1118 - 1122 (2021/02/16)

A chiral phosphoric acid-catalyzed enantioselective condensation of 2,2-disubstituted cyclobutane-1,3-diones with a primary amine is described. This reaction offered a mild and efficient protocol for constructing quaternary carbon-containing cyclobutanes

A simple method for the synthesis of 2-amino-1(4′-methoxyphenyl)-propane

Mereyala,Koduru

, p. 3005 - 3010 (2007/10/03)

Synthesis of 2-amino-1-(4′-methoxyphenyl)-propane (II) starting from p-anisaldehyde (1) in 67% overall yield is described. Key reactions involved Horner-Wadswoth-Emmons olefination of 1 to form the ester 2 and Hoffmann degradation of amide 5 to obtain the amine II.

Convenient Synthetic Sequence for the Preparation of Indanones

Smonou, Ioulia,Orfanopoulos, Michael

, p. 1387 - 1397 (2007/10/02)

A convenient and general methods is reported for the synthesis of indanones from aryl ketones or aldehydes.

Syntheses of 5-, 7-, and 8-Methoxy-3-methyl-2-tetralone

Johansson, Anette M.,Mellin, Charlotta,Hacksell, Uli

, p. 5252 - 5258 (2007/10/02)

Two efficient syntheses of 5-methoxy- and 8-methoxy-3-methyl-2-tetralone and the synthesis of the 7-methoxy isomer via a different route are described.Also reported is the synthesis of 8-methoxy-3,3-dimethyl-2-tetralone.The regioselectivity of lithium carbanion formation in 1,6-, 1,7-, and 2,7-dihydroxynaphthalene is discussed.The latter compound undergoes dimetalation more easily than the other isomers.

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