132062-74-9 Usage
### Main Properties
1. Chemical Name:
2-amino-9-[(2R,6R)-6-(hydroxymethyl)-1,4-oxathian-2-yl]-3,9-dihydro-6H-purin-6-one
2. Molecular Structure:
Complex molecular structure
3. Components:
Purine base
Amino group
Oxathiane ring
Hydroxymethyl group
4. Potential Biological Activity:
Due to the purine moiety, which is present in important nucleic acids like DNA and RNA
5. Chemical and Pharmaceutical Properties:
Imparted by the oxathiane ring and hydroxymethyl group
6. Research Status:
Further research and analysis are necessary to fully understand its potential uses and effects
### Specific Content
1. Purine Base:
Role:
Present in important nucleic acids like DNA and RNA
Chemical Structure:
Derived from the parent purine structure
2. Amino Group:
Role:
Provides basic properties and potential reactivity in chemical reactions
Chemical Structure:
NH2 group attached to the purine base
3. Oxathiane Ring:
Role:
Unique chemical structure that can impart specific properties to the compound
Chemical Structure:
1,4-oxathian-2-yl group
Specific Feature:
Contains a hydroxymethyl group attached to the 6-position of the oxathiane ring
4. Hydroxymethyl Group:
Role:
Can influence the compound's solubility, stability, and reactivity
Chemical Structure:
CH2OH group attached to the oxathiane ring
This breakdown covers the main properties and specific components of the chemical compound, providing a comprehensive understanding of its molecular structure and potential biological and pharmaceutical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 132062-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,6 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132062-74:
(8*1)+(7*3)+(6*2)+(5*0)+(4*6)+(3*2)+(2*7)+(1*4)=89
89 % 10 = 9
So 132062-74-9 is a valid CAS Registry Number.
132062-74-9Relevant articles and documents
NUCLEOSIDE ANALOGUES WITH A 1,4-DIOXANE, 1,4-OXATHIANE OR 1,4-OXAZINE RING STRUCTURE AS THE CARBOHYDRATE FRAGMENT
Aerschot, Arthur Van,Janssen, Gerard,Herdewijn, Piet
, p. 769 - 777 (2007/10/02)
Pyrimidine and purine nucleoside analogues with a 1,4-dioxane, 1,4-oxathiane or 1,4-oxazine ring structure have been prepared from the corresponding dimesylated seconucleosides by treatment with either sodium hydroxide, sodium sulfide or primary alkylamines.
