90057-07-1 Usage
Description
6-Hydroxy-2-methoxy-7-deazapurine, with the chemical formula C6H6N4O3, is an off-white solid compound that plays a significant role in organic synthesis. It is characterized by the presence of a hydroxyl group at the 6th position, a methoxy group at the 2nd position, and the absence of an amino group at the 7th position, which differentiates it from traditional purine structures.
Uses
Used in Organic Synthesis:
6-Hydroxy-2-methoxy-7-deazapurine is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the formation of diverse chemical entities through reactions such as nucleophilic substitution, electrophilic addition, and rearrangement reactions. This versatility makes it a valuable building block for the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-Hydroxy-2-methoxy-7-deazapurine is utilized as a precursor for the synthesis of novel drug candidates. Its unique structural features enable the design of molecules with potential therapeutic applications, such as antiviral, anticancer, and anti-inflammatory agents. 6-HYDROXY-2-METHOXY-7-DEAZAPURINE's reactivity and functional group compatibility make it an attractive starting material for medicinal chemists to explore new drug discovery avenues.
Used in Agrochemical Industry:
6-Hydroxy-2-methoxy-7-deazapurine also finds application in the agrochemical industry, where it serves as a starting material for the synthesis of bioactive molecules with potential use as pesticides, herbicides, and plant growth regulators. Its ability to form a wide range of derivatives makes it a valuable asset in the development of new agrochemical products with improved efficacy and selectivity.
Used in Research and Development:
In the realm of research and development, 6-Hydroxy-2-methoxy-7-deazapurine is employed as a model compound for studying various chemical reactions and mechanisms. Its unique structure provides insights into the reactivity and selectivity of different functional groups, contributing to the advancement of organic chemistry and related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 90057-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,5 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90057-07:
(7*9)+(6*0)+(5*0)+(4*5)+(3*7)+(2*0)+(1*7)=111
111 % 10 = 1
So 90057-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O2/c1-12-7-9-5-4(2-3-8-5)6(11)10-7/h2-3H,1H3,(H2,8,9,10,11)
90057-07-1Relevant articles and documents
Synthesis, anticancer and antimicrobiological activities of pyrrolo[2,3-d]pyrimidines
Quijano,Nogueras,Sanchez,Alvarez de Cienfuegos,Melgarejo
, p. 1079 - 1083 (2007/10/02)
Reactions of 6-amino-3,4-dihydro-2-methoxy-4-oxopyrimidine 1a and its 3-methyl derivative 1b with chloroacetaldehyde and chloroacetyl chloride are discussed in this paper. Amongst others compounds, we have obtained, in low yield, the novel ring system oxazolo[3,2-c]pyrrolo[3,2-e]pyrimidine. The anticancer and anti-microbial activities of some of the obtained products are described.
