769951-32-8 Usage
General Description
7H-Pyrrolo[2,3-d]pyrimidin-4-amine sulphate is a chemical compound that comes under the class of pyrrolopyrimidine. With a molecular formula of C7H7N5.H2SO4, this specific compound is characterized by the fusion of a pyrrole ring and a pyrimidine ring. These types of compounds are known for their wide range of biological activities. In addition, 7H-Pyrrolo[2,3-d]pyrimidin-4-amine sulphate is potentially useful for synthesis in chemical research. Detailed safety, toxicity, or environmental impact data for this chemical is not readily available, indicating that it may not be extensively studied or generally utilized in various industries.
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 articles and documents
Practical synthesis of a potent hepatitis C virus RNA replication inhibitor
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.
