630107-95-8 Usage
Uses
Used in Pharmaceutical Industry:
Phosphonic acid, [[2-[[(4-methylphenyl)sulfonyl]oxy]ethoxy]methyl]-, bis(1-methylethyl) ester is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure and functional groups may contribute to the development of new drugs or drug delivery systems.
Used in Agrochemical Industry:
In the agrochemical industry, Phosphonic acid, [[2-[[(4-methylphenyl)sulfonyl]oxy]ethoxy]methyl]-, bis(1-methylethyl) ester is used as a component in the formulation of pesticides or herbicides. Its chemical properties may provide effective control of pests and weeds in agricultural settings.
Used in Materials Science:
Phosphonic acid, [[2-[[(4-methylphenyl)sulfonyl]oxy]ethoxy]methyl]-, bis(1-methylethyl) ester is used as a material in the development of new materials with specific properties. Its versatility in chemical structure allows for the creation of materials with tailored characteristics for various applications, such as in electronics or advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 630107-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,0,1,0 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 630107-95:
(8*6)+(7*3)+(6*0)+(5*1)+(4*0)+(3*7)+(2*9)+(1*5)=118
118 % 10 = 8
So 630107-95-8 is a valid CAS Registry Number.
630107-95-8Relevant academic research and scientific papers
Diversity oriented efficient access of trisubstituted purines via sequential regioselective Mitsunobu coupling and SNAr based C 6 functionalizations
Manvar, Atul,Shah, Anamik
, p. 680 - 691 (2013/07/25)
An efficient protocol for the syntheses of diverse 2,6,7- and 2,6,9-trisubstituted purines is reported starting from the guanine precursor, 2amino-6-chloropurine nucleoside through subsequent regioselective, high yielding Mitsunobu coupling and nucleophilic substitutions at C6 with versatile primary and secondary amines. A wide range of 2,6,7- and 2,6,9-trisubstituted purines were accessible in good to excellent yields with remarkable functional group tolerance. Moreover, solvent-free, large scale synthesis of precursors 2 & 3 and facile preparation of organophosphorus side chains 4 & 5 were also accomplished with excellent yields.
5-Substituted-2,4-diamino-6-[2-(phosphonomethoxy) ethoxy]pyrimidines-Acyclic Nucleoside Phosphonate Analogues with Antiviral Activity
Hocková, Dana,Holy, Antonín,Masojídková, Milena,Andrei, Graciela,Snoeck, Robert,De Clercq, Erik,Balzarini, Jan
, p. 5064 - 5073 (2007/10/03)
2,4-Diamino-6-hydroxypyrimidines substituted in position 5 by an allyl, benzyl, cyanomethyl, ethoxycarbonylmethyl, phenyl, cyclopropyl, or methyl group were prepared either by C5-alkylation or by formation of the pyrimidine ring by cyclization. Their alky
