769951-32-8 Usage
Uses
Used in Chemical Research:
7H-Pyrrolo[2,3-d]pyrimidin-4-amine sulphate is used as a synthetic intermediate for the development of new compounds in chemical research. Its unique structure and potential biological activities make it a valuable candidate for further exploration and application in various fields.
Used in Pharmaceutical Industry:
7H-Pyrrolo[2,3-d]pyrimidin-4-amine sulphate is used as a potential drug candidate for the development of new therapeutic agents. Its wide range of biological activities suggests that it may have potential applications in the treatment of various diseases and conditions.
Used in Material Science:
7H-Pyrrolo[2,3-d]pyrimidin-4-amine sulphate is used as a building block for the synthesis of novel materials with unique properties. Its chemical structure and reactivity may contribute to the development of advanced materials for various applications, such as electronics, sensors, or energy storage devices.
Check Digit Verification of cas no
The CAS Registry Mumber 769951-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,9,9,5 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 769951-32:
(8*7)+(7*6)+(6*9)+(5*9)+(4*5)+(3*1)+(2*3)+(1*2)=228
228 % 10 = 8
So 769951-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4.H2O4S/c7-5-4-1-2-8-6(4)10-3-9-5;1-5(2,3)4/h1-3H,(H3,7,8,9,10);(H2,1,2,3,4)
769951-32-8Relevant academic research and scientific papers
Bio, Matthew M.,Xu, Feng,Waters, Marjorie,Williams, J. Michael,Savary, Kimberly A.,Cowden, Cameron J.,Yang, Chunhua,Buck, Elizabeth,Song, Zhiguo J.,Tschaen, David M.,Volante,Reamer, Robert A.,Grabowski, Edward J. J.
, p. 6257 - 6266 (2004)
A practical, efficient synthesis of 1, a hepatitis C virus RNA replication inhibitor, is described. Starting with the inexpensive diacetone glucose, the 12-step synthesis features a novel stereoselective rearrangement to prepare the key crystalline furanose diol intermediate. This is followed by a highly selective glycosidation to couple the C-2 branched furanose epoxide with deazapurine.
