100047-45-8 Usage
General Description
2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI) is a chemical compound with the molecular formula C6H7N3O. It is a heterocyclic compound containing a pyrrolopyrimidine ring system and an amino group. 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI) has potential medicinal properties and may be used in the development of pharmaceutical drugs. It may also have applications in organic synthesis and chemical research. Overall, 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI) is a versatile chemical compound with a range of potential uses in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 100047-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,4 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100047-45:
(8*1)+(7*0)+(6*0)+(5*0)+(4*4)+(3*7)+(2*4)+(1*5)=58
58 % 10 = 8
So 100047-45-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4O/c7-4-3-1-2-8-5(3)10-6(11)9-4/h1-2H,(H4,7,8,9,10,11)
100047-45-8Relevant articles and documents
Furanoside-Pyranoside Isomerization of Tubercidin and its 2'-Deoxy Derivatives: Influence of Nucleobase and Sugar Structure on the Proton-catalysed Reaction
Seela, Frank,Menkhoff, Sabine,Behrendt, Silvia
, p. 525 - 530 (2007/10/02)
2'-Deoxy-2-methoxytubercidin (6a) which was prepared from the nucleobase (1a) with the halogenose (2) via phase-transfer glycosylation isomerizes rapidly under acidic conditions.Two pyranosides and the anomeric furanoside (5a) are formed.The isomerization process was followed kinetically, demonstrating that furanoside formation is kinetically controlled whereas the β-pyranoside (7a) is the thermodynamically most stable product.From 2'-deoxytubercidin (6b) similar results were obtained but isomerization was slow, compared with (6a).The ribonucleoside tubercidin (6c) did isomerize only under vigorous acid treatment leading to the α-furanoside (5c) and the nucleobase (1c) by cleavage of the N-glycosylic bond.