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(4-methoxy)phenyl propyl sulfoxide is an organic compound characterized by its molecular formula C10H14O2S. It features a phenyl ring with a methoxy group (-OCH3) at the para position (4th position), and a propyl sulfoxide group attached to it. The propyl sulfoxide group consists of a propyl chain (three carbon atoms) with a sulfoxide (-SO) group at the terminal carbon. (4-methoxy)phenyl propyl sulfoxide is known for its unique chemical properties, such as its ability to act as a chiral auxiliary in asymmetric synthesis, and it is also used in the preparation of various pharmaceuticals and agrochemicals due to its potential to influence the stereochemistry of reactions. The compound's structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules.

21865-10-1

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21865-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21865-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21865-10:
(7*2)+(6*1)+(5*8)+(4*6)+(3*5)+(2*1)+(1*0)=101
101 % 10 = 1
So 21865-10-1 is a valid CAS Registry Number.

21865-10-1Downstream Products

21865-10-1Relevant academic research and scientific papers

A mild and chemoselective CALB biocatalysed synthesis of sulfoxides exploiting the dual role of AcOEt as solvent and reagent

Anselmi, Silvia,Liu, Siyu,Kim, Seong-Heun,Barry, Sarah M.,Moody, Thomas S.,Castagnolo, Daniele

supporting information, p. 156 - 161 (2021/01/14)

A mild, chemoselective and sustainable biocatalysed synthesis of sulfoxides has been developed exploiting CALB and using AcOEt with a dual role of more environmentally friendly reaction solvent and enzyme substrate. A series of sulfoxides, including the drug omeprazole, have been synthesised in high yields and with excellent E-factors.

Efficient aerobic oxidation of phosphines, phosphites, and sulfides by using trialkylborane

Motoshima, Kosuke,Sato, Akinori,Yorimitsu, Hideki,Oshima, Koichiro

experimental part, p. 2229 - 2231 (2009/08/08)

Treatment of phosphines, phosphites, or sulfides with trialkylborane under air afforded the corresponding oxides in good yields.

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