63838-48-2 Usage
Uses
Used in Pharmaceutical Industry:
2-azabicyclo(2.2.1)hept-5-en-3-one serves as a crucial precursor and intermediate in the synthesis of various pharmaceuticals. Its role in the development of antiviral and antifungal agents is particularly noteworthy, given its ability to contribute to the creation of life-saving medications.
Used in Agrochemical Industry:
Beyond human healthcare, 2-azabicyclo(2.2.1)hept-5-en-3-one also plays a significant role in agriculture. It is utilized in the production of insecticides and herbicides, helping to protect crops from pests and weeds, thereby ensuring food security and agricultural productivity.
Used in Organic Synthesis:
The unique structure and reactivity of 2-azabicyclo(2.2.1)hept-5-en-3-one make it a valuable building block in organic synthesis. Its applications extend to the creation of complex organic compounds, contributing to advancements in chemical research and the development of new materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 63838-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63838-48:
(7*6)+(6*3)+(5*8)+(4*3)+(3*8)+(2*4)+(1*8)=152
152 % 10 = 2
So 63838-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO/c8-6-4-2-1-3-5(4)7-6/h1,3-5H,2H2,(H,7,8)
63838-48-2Relevant academic research and scientific papers
Novel 1,2-disubstituted carbocyclic nucleoside analogues of purine with a cyclopentene ring
Besada,Gonzalez-Moa,Teran,Santana,Uriarte
, p. 2445 - 2449 (2007/10/03)
A total and versatile synthesis of a new series of carbocyclic nucleoside analogues which are derivatives of purine with a 1,2-disubstituted cyclopentene ring (I) is described. The 6-chloropurine derivatives 3 and 9 were prepared by construction of the heterocyclic base about the primary amino group of the (±)-cis-2-amino-3-cyclopentenylmethanol (1), which was synthesized in good yield from cyclopentadiene in four steps. The substitution of a chlorine atom in the compounds 3 and 9 by an amino group (compounds 4 and 10) and by a hydroxyl group (compounds 5 and 11) was carried out with NH4OH or with NaOH, respectively.
