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63838-48-2

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63838-48-2 Usage

General Description

2-azabicyclo(2.2.1)hept-5-en-3-one, also known as 6-oxo-3-azabicyclo[3.1.0]hexane, is a bicyclic lactam compound with a nitrogen atom in its ring structure. It is commonly used as a precursor and intermediate in the synthesis of pharmaceuticals and agrochemicals. 2-azabicyclo(2.2.1)hept-5-en-3-one has a wide range of applications, including as a building block in the preparation of various pharmaceuticals such as antiviral and antifungal agents, as well as in the production of insecticides and herbicides. Its unique structure and reactivity make it a valuable component in organic synthesis and chemical manufacturing.

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 articles and documents

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.

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