1928-77-4 Usage
Description
6-CHLORO-7-BENZYLPURINE is an organic compound that serves as a valuable intermediate in the synthesis of 1-substituted adenines. It is a white solid with significant potential in various chemical and pharmaceutical applications due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
6-CHLORO-7-BENZYLPURINE is used as a key intermediate for the synthesis of 1-substituted adenines, which are essential components in the development of various pharmaceutical products. Its role in the synthesis process is crucial for creating new and innovative medications that can address a wide range of health concerns.
Used in Chemical Synthesis:
In the field of chemical synthesis, 6-CHLORO-7-BENZYLPURINE is utilized as an important building block for creating a variety of complex organic molecules. Its unique structure and reactivity make it a valuable asset in the development of new compounds with diverse applications, including but not limited to, materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
6-CHLORO-7-BENZYLPURINE is also employed in research and development settings, where it is used to explore new chemical reactions and pathways. Its versatility as a synthetic intermediate allows researchers to investigate novel approaches to drug discovery and the creation of advanced materials with improved properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1928-77-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1928-77:
(6*1)+(5*9)+(4*2)+(3*8)+(2*7)+(1*7)=104
104 % 10 = 4
So 1928-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H9ClN4/c13-11-10-12(15-7-14-11)16-8-17(10)6-9-4-2-1-3-5-9/h1-5,7-8H,6H2
1928-77-4Relevant articles and documents
Regioselective alkylation reaction of purines under microwave irradiation
Ginard, Jaume,Jahani, Daniel,Mur, Nuria,Pujol, Maria Dolors,Vi?as, Miquel,Vinuesa, Arturo
, (2021/12/22)
The alkylation of purines which is generally carried out after anion formation by treatment with a base and alkyl halide is complicated and in the best cases, mixtures of N-alkylated compounds are obtained. Purine derivatives can be acquired from alkylati
METHOD FOR SYNTHESIZING DIVERSELY SUBSTITUTED PURINES
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Page/Page column 34, (2018/12/03)
The present invention relates to a method for synthesizing diversely substituted purines starting from a pyrimidine. Formula (I). The method comprises the formation of an amidine group on the pyrimidine by implementing a Vilsmeier type reagent, the functi
Direct, Regioselective N-Alkylation of 1,3-Azoles
Chen, Shuai,Graceffa, Russell F.,Boezio, Alessandro A.
supporting information, p. 16 - 19 (2016/01/15)
Regioselective N-alkylation of 1,3-azoles is a valuable transformation. Organomagnesium reagents were discovered to be competent bases to affect regioselective alkylation of various 1,3-azoles. Counterintuitively, substitution selectively occurred at the more sterically hindered nitrogen atom. Numerous examples are provided, on varying 1,3-azole scaffolds, with yields ranging from 25 to 95%.