97174-13-5 Usage
Uses
Used in Plastics Industry:
Phosphoric acid dibenzyl ester, sodium-salt is used as a flame retardant for plastics to enhance their fire resistance and safety in various applications.
Used in Rubber Industry:
In the rubber industry, sodium dibenzyl phosphate is used as a flame retardant to improve the fire safety of rubber products, such as cables, hoses, and seals.
Used in Textile Industry:
Sodium dibenzyl phosphate is used as a flame retardant in textiles to provide fire resistance to fabrics used in clothing, upholstery, and other textile products.
Used as a Plasticizer:
Phosphoric acid dibenzyl ester, sodium-salt is used as a plasticizer to increase the flexibility and workability of certain materials, improving their performance in various applications.
Used as an Anti-corrosive Agent:
Sodium dibenzyl phosphate is utilized as an anti-corrosive agent in industrial applications to protect materials from corrosion and extend their service life.
Safety Precautions:
It is important to handle phosphoric acid dibenzyl ester, sodium-salt with care and follow safety precautions, as exposure to high concentrations can cause irritation to the skin, eyes, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 97174-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97174-13:
(7*9)+(6*7)+(5*1)+(4*7)+(3*4)+(2*1)+(1*3)=155
155 % 10 = 5
So 97174-13-5 is a valid CAS Registry Number.
97174-13-5Relevant academic research and scientific papers
Prodrugs of Phosphonoformate: Products, Kinetics and Mechanisms of Hydrolysis of Dibenzyl (Methoxycarbonyl)phosphonate
Mitchell, Antony G.,Nicholls, Dave,Walker, Ian,Irwin, William J.,Freeman, Sally
, p. 1297 - 1304 (2007/10/02)
Dibenzyl (methoxycarbonyl)phosphonate (1) has been prepared by the reaction of benzyl alcohol with (methoxycarbonyl)phosphonic dichloride.The hydrolysis of 1 proceeded rapidly, with a half-life of 60 min at 36.4 deg C and pH 7.4, by two main pathways.The dominant pathway (k1, 6.56 * 10-3 min-1) yielded the diester, benzyl (methoxycarbonyl)phosphonate (2) and benzyl alcohol (3), with P-O cleavage.The second (k2, 3.55 * 10-3 min-1) gave dibenzyl phosphite (4), possibly arising from the hydrolysis of the carboxyl ester followed by decarboxylation.Benzyl phosphite (5) was also observed, which arises from the hydrolysis of 4 with P-O cleavage (k5, 9.04 * 10-4 min-1).Other products formed in small amounts were, benzyl (benzyloxycarbonyl)phosphonate (6) (k3, 3.59 * 10-4 min-1) and dibenzyl phosphate (7) (k4, 4.24 * 10-4 min-1).The rapid and complicated hydrolysis of 1, involving four competitive reactions, two of which involve C-P bond cleavage, suggests that triesters of phosphonoformate are unlikely to be suitable prodrug forms.
