630107-95-8 Usage
General Description
Phosphonic acid, [[2-[[(4-methylphenyl)sulfonyl]oxy]ethoxy]methyl]-, bis(1-methylethyl) ester is a complex chemical compound with multiple functional groups. It is comprised of a phosphonic acid core, along with ester and sulfonyl groups. The chemical structure features two isopropyl (1-methylethyl) ester groups, which are organic compounds commonly used as solvents and in the production of flavoring additives and fragrances. The sulfonyl group is a functional group containing a sulfur atom, with the compound also containing an ethoxy group. Overall, this chemical compound has widespread applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Due to its complexity and multiple functional groups, it is essential that the compound is handled and used with appropriate safety precautions.
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 articles and documents
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.
