Welcome to LookChem.com Sign In|Join Free
  • or
diethyl N-benzoyl-α-aminomethylphosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20495-33-4

Post Buying Request

20495-33-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

20495-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20495-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,9 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20495-33:
(7*2)+(6*0)+(5*4)+(4*9)+(3*5)+(2*3)+(1*3)=94
94 % 10 = 4
So 20495-33-4 is a valid CAS Registry Number.

20495-33-4Relevant academic research and scientific papers

A new way for potential aminophosphonic acids precursors

Cristau, Henri-Jean,Lambert, Jean-Marc,Sarris, Anne,Pirat, Jean-Luc

, p. 125 (2007/10/03)

New five membered-ring 3,3-dihydro-1,4,2-oxazaphospholenes 1, potential precursors of aminophosphonic acids, have been synthesized and characterized by 1H, 13C and 31P NMR.

Convenient Preparations of Diethyl phosphonates, 2-Azabutadienes, and Isoquinolines from a 1,2-Monoazabisylide Equivalent

Katritzky, Alan R.,Zhang, Guifen,Jiang, Jinlong

, p. 4556 - 4560 (2007/10/02)

Diethyl methyl>phosphonate (4), prepared in situ by treatment of 1-methyl>benzotriazole (betmip 6) with diethyl phosphite anion, is converted by treatment with butyllithium into the corresponding carbanion 5.Carbanion 5, the first example of a 1,2-monoazabisylide equivalent, provides a versatile synthetic method to introduce the C=NC=C structural unit, as illustrated by convenient preparations of 1,4-diaryl-2-azabutadienes, 1,1,4,4-tetraaryl-2-azabutadienes, diethyl phosphonates, and isoquinolines.

CONVERSION OF AMINO ACIDS AND DIPEPTIDES INTO THEIR PHOSPHONIC ANALOGS; Aminoalkylphosphonic acids and peptides II.

Oesapay, George,Szilagyi, Ildiko,Seres, Jenoe

, p. 2977 - 2984 (2007/10/02)

Acylamino carboxylic acids were degradated by the Hunsdiecker-reaction; the bromo-derivatives were reacted with NaPO(OC2H5)2.Aminophosphonic acids were obtained by acidic hydrolysis, and half-blocked derivatives by the selective removal of masking substituents.Two phosphonopeptides were also prepared by this route.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 20495-33-4