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Phosphoric acid, 2-oxo-2-phenylethyl diphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16222-22-3

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16222-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16222-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,2 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16222-22:
(7*1)+(6*6)+(5*2)+(4*2)+(3*2)+(2*2)+(1*2)=73
73 % 10 = 3
So 16222-22-3 is a valid CAS Registry Number.

16222-22-3Downstream Products

16222-22-3Relevant academic research and scientific papers

Novel oxidative α-tosyloxylation of alcohols with iodosylbenzene and p-toluenesulfonic acid and its synthetic use for direct preparation of heteroaromatics

Ueno, Makoto,Nabana, Takahiro,Togo, Hideo

, p. 6424 - 6426 (2003)

α-Tosyloxyketones and α-tosyloxyaldehydes were directly prepared from alcohols by treatment with iodosyl-benzene and p-toluenesulfonic acid monohydrate in good yields. This method can be used for the direct preparation of thiazoles, imidazoles, and imidaz

REGIOSPECIFIC CONVERSION OF TERMINAL ALKYNES TO KETOL PHOSPHATES WITH AN IODINE(III)-PHOSPHATE REAGENT

Koser, Gerald F.,Chen, Xiao,Chen, Kuanchiang,Sun, Guoping

, p. 779 - 782 (1993)

Terminal alkynes undergo regiospecific conversion to ketol phosphates when treated with the iodine(III)-phosphate 2 in acetonitrile containing water.

An efficient microwave-promoted solvent-free α-phosphoryloxylation of ketones

Pu, Ye,Fang, Yingguo,Yan, Jie

, p. 522 - 525 (2012/11/07)

An efficient solvent-free α-phosphoryloxylation of ketones under microwave irradiation is reported. When ketones reacted with phosphates and (diacetoxyiodo)benzene under microwave irradiation for short time, the α-phosphoryloxylaction of ketones was easil

An effective catalytic α-phosphoryloxylation of ketones with iodobenzene

Pu, Ye,Gao, Liumian,Liu, Huijun,Yan, Jie

experimental part, p. 99 - 103 (2012/03/26)

An effective catalytic method for α-phosphoryloxylation of ketones is reported. When ketones were reacted with phosphates in the presence of iodobenzene as the recyclable catalyst and m-chloroperbenzoic acid as the terminal oxidant in acetonitrile at room temperature, the α- phosphoryloxylation of ketones took place easily and the corresponding keto phosphates were obtained in moderate to good yields. Georg Thieme Verlag Stuttgart. New York.

Reactivities of novel [hydroxy(tosyloxy)iodo]arenes and [hydroxy(phosphoryloxy)iodo]arenes for α-tosyloxylation and α-phosphoryloxylation of ketones

Nabana, Takahiro,Togo, Hideo

, p. 4362 - 4365 (2007/10/03)

Novel [hydroxy(tosyloxy)iodo]arenes bearing 2-thienyl, 3-thienyl, N-tosyl-4-pyrazolyl, 3-trifluoromethylphenyl, and 3,5-bis(trifiuoromethy)phenyl as an aromatic group, and [hydroxy(phosphoryloxy)iodo]arenes bearing N. tosyl-4-pyrazolyl, 3-trifluoromethylp

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