56317-74-9 Usage
Uses
Used in Water Treatment:
Phosphonic acid, mono(phenylmethyl) ester, ammonium salt is used as a chelating agent for [preventing metal ion precipitation and interference in water treatment processes].
Used in Metal Treatment:
Phosphonic acid, mono(phenylmethyl) ester, ammonium salt is used as a chelating agent for [preventing metal ion precipitation and interference in metal treatment processes].
Used in Detergent and Cleaning Agent Production:
Phosphonic acid, mono(phenylmethyl) ester, ammonium salt is used as a chelating agent for [enhancing the cleaning and detergent properties by preventing metal ion interference].
Used as a Hydrogen Peroxide Stabilizer:
Phosphonic acid, mono(phenylmethyl) ester, ammonium salt is used as a stabilizer for [preventing the decomposition of hydrogen peroxide in various industrial applications].
Used as a Corrosion Inhibitor:
Phosphonic acid, mono(phenylmethyl) ester, ammonium salt is used as a corrosion inhibitor for [protecting metal surfaces from corrosion in various industries].
Used in Agriculture:
Phosphonic acid, mono(phenylmethyl) ester, ammonium salt is used in the formulation of herbicides and pesticides for [enhancing their effectiveness and preventing metal ion interference in agricultural applications].
Check Digit Verification of cas no
The CAS Registry Mumber 56317-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,1 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56317-74:
(7*5)+(6*6)+(5*3)+(4*1)+(3*7)+(2*7)+(1*4)=129
129 % 10 = 9
So 56317-74-9 is a valid CAS Registry Number.
56317-74-9Relevant academic research and scientific papers
Kers,Kers,Stawinski,Sobkowski,Kraszewski
, p. 427 - 430 (1995)
A simple and efficient synthetic method for the preparation of alkyl H-phosphonate monoesters has been developed. The method consists of transesterification of commercially available diphenyl H-phosphonate with an appropriate alcohol under mild conditions, followed by ammonolysis of the in situ formed dialkyl and alkyl phenyl H-phosphonates.
New access to H-phosphonates via metal-catalyzed phosphorus-oxygen bond formation
Coudray, La?titia,Abrunhosa-Thomas, Isabelle,Montchamp, Jean-Luc
, p. 6505 - 6508 (2008/02/12)
A novel approach to H-phosphonates from hypophosphorous acid using a transfer hydrogenation process was developed. This method is atom-economical, environmentally friendly, catalytic, and efficient, leading easily to H-phosphonate monoesters or ammonium s
Phosphorylation of benzyl-protected sugar derivatives via 1-h-phosphonate intermediates: Synthesis of dl-myo-inositol 1,4,5-tris-1-h-phosphonate
Dreef,van der Marel,van Boom
, p. 512 - 513 (2007/10/02)
The crystalline and easily accessible ammonium salt of benzyl-1-H-phosphonic acid has been used for the formation of intermediate benzyl-1-H-phosphonate diester bonds between primary, secondary and anomerically HO-groups of benzyl-protected (pseudo)sugar derivatives. These intermediates proved to be very suitable for the preparation of modified and non-modified phosphate functions.
