75499-99-9 Usage
Uses
Used in Organic Synthesis:
2,4(1H,3H)-Pyrimidinedione, 1,3-bis[(phenylmethoxy)methyl]is used as a reagent in organic synthesis for its ability to facilitate the formation of new compounds with potential biological activity. Its unique structure allows for the creation of diverse chemical entities, contributing to the advancement of chemical research and development.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,4(1H,3H)-Pyrimidinedione, 1,3-bis[(phenylmethoxy)methyl]serves as a building block for the synthesis of new compounds with potential therapeutic applications. Its structure and properties make it a promising candidate for the development of innovative drugs, addressing unmet medical needs and improving patient outcomes.
Used in Agrochemical Development:
2,4(1H,3H)-Pyrimidinedione, 1,3-bis[(phenylmethoxy)methyl]also finds application in the agrochemical sector, where it is utilized as a starting material for the synthesis of new agrochemicals. Its unique structure and properties enable the development of novel compounds with potential applications in crop protection, pest control, and other agricultural areas, contributing to sustainable agriculture and food security.
Check Digit Verification of cas no
The CAS Registry Mumber 75499-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,9 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75499-99:
(7*7)+(6*5)+(5*4)+(4*9)+(3*9)+(2*9)+(1*9)=189
189 % 10 = 9
So 75499-99-9 is a valid CAS Registry Number.
75499-99-9Relevant academic research and scientific papers
Synthesis of chiral carbocyclic ribonucleotides
Antle, Vincent D.,Caperelli, Carol A.
, p. 1911 - 1928 (2007/10/03)
The carbocyclic analogs of CMP, UMP, GMP, IMP, and ribo-TMP, of the same absolute configuration as the naturally occurring β-D-ribofuranose-based ribonucleoside monophosphates, have been synthesized. The synthetic route employed Mitsunobu coupling of the
A new synthesis of n-blocked dihydrouracil and dihydroorotic acid derivatives using lithium tri-sec-butyl borohydride as reducing agent
Hannon, Stephen J.,Kundu, Nitya G.,Hertzberg, Robert P.,Bhatt, Ram S.,Heidelberger, Charles
, p. 1105 - 1108 (2007/10/02)
1,3-Di-N-substituted uracil and its derivatives have been reduced with lithium-tri-sec-butyl borohydride to the corresponding 5,6-dihydro compounds in excellent yields. Alkylation of 5-position of uracil is also very conveniently accomplished.
