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Phosphoric acid, 3,4-dimethylphenyl diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14143-06-7

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14143-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14143-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,4 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14143-06:
(7*1)+(6*4)+(5*1)+(4*4)+(3*3)+(2*0)+(1*6)=67
67 % 10 = 7
So 14143-06-7 is a valid CAS Registry Number.

14143-06-7Downstream Products

14143-06-7Relevant academic research and scientific papers

Triethylphosphate/phosphorus pentoxide as an efficient reagent for the phosphorylation of phenols

Kaboudin, Babak,Mostafalu, Ramin

, p. 776 - 780 (2012)

A simple, efficient, and novel method has been developed for the phosphorylation of phenols. Treatment of phenols with a mixture of triethylphosphate/phosphorus pentoxide gives the corresponding phosphate derivatives in good yields. This method is easy, rapid, and offers good yields for the phosphorylation of phenols. The reaction of triethylphosphate with phosphorus pentoxide was also studied by variable-temperature 31P-NMR spectroscopy. Copyright

Enantioselective and Regioselective Hydroetherification of Alkynes by Gold-Catalyzed Desymmetrization of Prochiral Phenols with P-Stereogenic Centers

Zheng, Yin,Guo, Linna,Zi, Weiwei

supporting information, p. 7039 - 7043 (2018/11/24)

The gold(I)-catalyzed enantioselective hydroetherification of alkynes was achieved via desymmetrization of prochiral bisphenols bearing P-stereogenic centers. (S)-DTBM-Segphos(AuCl)2/AgNTf2 proved to be a highly efficient catalyst system for this transformation, affording P-chiral cyclic phosphine oxides in good yields with high enantioselectivities (with up to 99% ee). The same catalyst system allowed for the enantioselective desymmetrization of dialkynes. Synthetic transformations of the cyclization products afforded other P-chiral molecules with high enantiospecificity.

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