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α-Propionyloxy-deoxybenzoin is a chemical compound with the molecular formula C12H14O4. It is a derivative of deoxybenzoin, featuring a propionyloxy group (-CH2CH2COO-) attached to the α-carbon position. α-propionyloxy-deoxybenzoin is often used as a protecting group in organic synthesis, particularly in the protection of alcohols and phenols. The propionyloxy group can be selectively removed under mild acidic conditions, making it a valuable tool for chemists in the synthesis of complex molecules. Its stability and ease of removal contribute to its utility in various chemical transformations, such as in the preparation of pharmaceuticals and other specialty chemicals.

53901-50-1

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53901-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53901-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,0 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53901-50:
(7*5)+(6*3)+(5*9)+(4*0)+(3*1)+(2*5)+(1*0)=111
111 % 10 = 1
So 53901-50-1 is a valid CAS Registry Number.

53901-50-1Downstream Products

53901-50-1Relevant academic research and scientific papers

Ceric ammonium nitrate promoted oxidation of oxazoles

Evans, David A.,Nagorny, Pavel,Xu, Risheng

, p. 5669 - 5671 (2007/10/03)

The ceric ammonium nitrate promoted oxidations of 4,5-diphenyloxazoles and oxazoles with various substitution patterns have been investigated. This transformation results in the formation of the corresponding imide in good yield and tolerates a wide variety of functional groups and substituents on the oxazole moiety.

Convenient syntheses of 2-alkyl(Aryl)-4,5-diphenyloxazoles and 2-alkyl(Aryl)-4-phepyloxazoles

Pei, Weiwei,Li, Shaohui,Nie, Xiaoping,Li, Yiwei,Pei, Jian,Chen, Bingzi,Wu, Jie,Ye, Xiulin

, p. 1298 - 1304 (2007/10/03)

The synthetic methods to prepare 2-alkyl(aryl)-4,5-diphenyloxazoles and 2-alkyl(aryl)-4-phenyloxazoles were improved on the basis of a mechanistic study of oxazole formation from α-hydroxy ketones (carboxylic esters of benzoin and phenacyl alcohols). By these methods, seven trisubstituted oxazoles and twelve disubstituted oxazoles of the title compounds were prepared.

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