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100047-45-8

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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)

100047-45-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-1,3-dihydropyrrolo[2,3-d]pyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 4-Amino-2-hydroxy-pyrrolo<2,3-d>pyrimidin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100047-45-8 SDS

100047-45-8Downstream Products

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.

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