162307-09-7 Usage
Description
2-Acetyl-2-azabicyclo[2.2.1]hept-5-en-3-one, commonly known as tropanone, is a bicyclic organic compound characterized by the presence of a five-membered and a seven-membered ring. It serves as a versatile intermediate in the synthesis of pharmaceutical compounds and complex organic molecules, leveraging its unique structural features and chemical properties.
Uses
Used in Pharmaceutical Industry:
2-Acetyl-2-azabicyclo[2.2.1]hept-5-en-3-one is used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly for the production of atropine and other tropane alkaloids. Its role in the development of these alkaloids is crucial due to its ability to serve as a building block in the creation of complex organic molecules with therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, 2-Acetyl-2-azabicyclo[2.2.1]hept-5-en-3-one is utilized as a starting material for the preparation of a wide range of chemical compounds. Its structural features and chemical properties make it a valuable component in the synthesis of diverse organic molecules, contributing to advancements in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 162307-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,0 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 162307-09:
(8*1)+(7*6)+(6*2)+(5*3)+(4*0)+(3*7)+(2*0)+(1*9)=107
107 % 10 = 7
So 162307-09-7 is a valid CAS Registry Number.
162307-09-7Relevant articles and documents
A practical enzymatic procedure for the resolution of N-substituted 2- azabicyclo[2.2.1]hept-5-en-3-one
Mahmoudian, Mahmoud,Lowdon, Andrew,Jones, Martin,Dawson, Michael,Wallis, Christopher
, p. 1201 - 1206 (1999)
A simple and efficient process for the enantioselective resolution of N- substituted 2-azabicyclo[2.2.1]hept-5-en-3-one has been developed using commercially available hydrolytic enzymes. This offers a practical approach for the preparation of enantiomerically pure N-substituted γ-lactams.
