81619-09-2 Usage
Description
(6-amino-3H-purin-3-yl)methyl 2,2-dimethylpropanoate is a chemical compound characterized by a purine ring, an amino group, and a methyl ester group. It is an organic compound with potential applications in various sectors due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Industry:
(6-amino-3H-purin-3-yl)methyl 2,2-dimethylpropanoate is used as a building block for the synthesis of various pharmaceutical compounds. Its purine ring and amino group can be utilized in the development of new drugs targeting specific biological pathways.
Used in Agricultural Industry:
(6-amino-3H-purin-3-yl)methyl 2,2-dimethylpropanoate is used as a chemical intermediate in the development of agrochemicals, such as pesticides and fertilizers. Its unique structure allows for the creation of novel compounds with improved efficacy and reduced environmental impact.
Used in Industrial Applications:
(6-amino-3H-purin-3-yl)methyl 2,2-dimethylpropanoate is used as a versatile intermediate in the synthesis of various industrial chemicals, including dyes, polymers, and additives. Its functional groups can be manipulated to create a wide range of products with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 81619-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,1 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81619-09:
(7*8)+(6*1)+(5*6)+(4*1)+(3*9)+(2*0)+(1*9)=132
132 % 10 = 2
So 81619-09-2 is a valid CAS Registry Number.
81619-09-2Relevant articles and documents
Electrophilic amination of adenines. Formation and characteristics of N-aminoadenines
Saga, Tetsuya,Kaiya, Toyo,Asano, Shoji,Kohda, Kohfuku
, p. 219 - 233 (1996)
Amination of adenine with H2N-O-SO3H in alkaline media afforded 1-, 3-, 7- and 9-aminoadenine isomers at a ratio of about 1:1:3:1. In neutral media, the product ratio of the isomers changed to about 3:1:1:0. These results were different from the regioselectivity obtained by methylation of adenine with dimethyl sulfate under similar conditions. Amination of adenine with dinitrophenoxyamine in DMF gave 1-aminoadenine as the main product and this regioselectivity was also different from that of methylation with CH3I. Chemical characteristics of these N-amino adenines are described.
