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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

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 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.

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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