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2,2-difluoro-1-phenylethyl diethyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83567-91-3

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83567-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83567-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,6 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83567-91:
(7*8)+(6*3)+(5*5)+(4*6)+(3*7)+(2*9)+(1*1)=163
163 % 10 = 3
So 83567-91-3 is a valid CAS Registry Number.

83567-91-3Downstream Products

83567-91-3Relevant academic research and scientific papers

Nucleophilic difluoromethylenation of aldehydes and ketones using diethyl difluoro(trimethylsilyl)methylphosphonate

Alexandrova, Anastasia V.,Beier, Petr

scheme or table, p. 493 - 500 (2009/12/06)

A new nucleophilic difluoromethylenation of aldehydes and ketones using diethyl difluoro(trimethylsilyl)methylphosphonate (1) has been achieved. The reactive carbanion species were generated under mild reaction conditions with a catalytic amount of initiator. This methodology was compatible with non-enolizable and in some cases with enolizable aldehydes and ketones and provided a straightforward access to phosphates of syn and anti 2,2-difluoro-1,3-diols.

An efficient and highly selective synthesis of (Z)-fluoroenol phosphates from hydroxy difluorophosphonates

Beier, Petr,Pohl, Radek,Alexandrova, Anastasia V.

experimental part, p. 957 - 962 (2009/12/03)

Substituted 2-aryl-2-hydroxy-1,1-difluorophosphonates undergo a reaction with potassium tert-butoxide to provide selectively (Z)-2-fluoro-1-arylvinyl phosphates in high yields. Georg Thieme Verlag Stuttgart.

Nucleophilic difluoromethylation and difluoromethylenation of aldehydes and ketones using diethyl difluoromethylphosphonate

Beier, Petr,Alexandrova, Anastasia V.,Zibinsky, Mikhail,Surya Prakash

scheme or table, p. 10977 - 10985 (2009/04/11)

New methodology for difluoromethylation and difluoromethylenation of aldehydes and ketones based on nucleophilic fluorination using diethyl difluoromethylphosphonate (1) was developed.

(DIETHYLPHOSPHINYL)DIFLUOROMETHYLLITHIUM. -PREPARATION AND SYNTHETIC APPLICATION-

Obayashi, Michio,Ito, Eiji,Matsui, Kiyohide,Kondo, Kiyosi

, p. 2323 - 2326 (2007/10/02)

The action of lithium diisopropylamide on diethyl difluoromethylphosphonate gives the title reagent which reacts with various electrophiles to introduce difluoromethylene or difluoromethyl unit.

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