30745-07-4 Usage
Description
[1,2,5]Oxadiazolo[3,4-d]pyrimidine-5,7-diamine, also known as ODP, is a chemical compound with the molecular formula C6H5N5O. It is a heterocyclic compound that contains both oxadiazole and pyrimidine rings. ODP is known for its unique electronic and photophysical properties, making it a versatile compound with potential applications in various fields.
Uses
Used in Pharmaceutical and Agrochemical Industries:
[1,2,5]Oxadiazolo[3,4-d]pyrimidine-5,7-diamine is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties allow for the development of new and effective compounds in these industries.
Used in Materials Science:
[1,2,5]Oxadiazolo[3,4-d]pyrimidine-5,7-diamine is used as a starting material for the synthesis of fluorescent dyes and photoactive materials. Its electronic and photophysical properties make it a promising candidate for applications in materials science.
Used in Biotechnology:
ODP has potential applications in the field of biotechnology due to its unique properties and reactivity. It can be utilized in the development of new biotechnological products and processes.
Used in Anticancer Applications:
[1,2,5]Oxadiazolo[3,4-d]pyrimidine-5,7-diamine has demonstrated potential as an anti-cancer drug candidate. It is used for its ability to inhibit certain enzymes involved in cancer cell proliferation, making it a promising compound for further research and development in the fight against cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 30745-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,4 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30745-07:
(7*3)+(6*0)+(5*7)+(4*4)+(3*5)+(2*0)+(1*7)=94
94 % 10 = 4
So 30745-07-4 is a valid CAS Registry Number.
30745-07-4Relevant articles and documents
Convenient and versatile synthetic methods for furazano[3,4-d]pyrimidines
Sako,Oda,Hirota,Beardsley
, p. 1255 - 1257 (2007/10/03)
Treatment of the readily available 6-amino-5-nitrosopyrimidines with a slight excess of iodobenzene diacetate or N-iodosuccinimide in anhydrous DMF containing three equivalents of lithium hydride at ambient temperature resulted in the smooth and versatile
