1223573-40-7 Usage
Chemical Family
Spiro-compounds
Explanation
Different sources of media describe the Explanation of 1223573-40-7 differently. You can refer to the following data:
1. Spiro-compounds are a class of organic compounds that contain two rings connected by a shared carbon atom. 1-Azaspiro[3.3]heptane, 1-(phenylMethyl)is a member of this family.
2. The bicyclic ring system refers to the two interconnected rings in the molecule. In this case, one of the rings contains a nitrogen atom, making it an azaspiro compound.
3. This is another way to name the compound, emphasizing the presence of a phenylmethyl (C6H5-CH2-) group attached to the nitrogen atom.
4. The compound is used as a starting material or intermediate in the synthesis of more complex organic molecules.
5. Research has shown that 1-Azaspiro[3.3]heptane, 1-(phenylMethyl)may have potential applications in the development of medications for treating depression and anxiety.
6. The compound is utilized in the creation of a range of industrial and scientific materials, highlighting its versatility and importance in chemical research and development.
Bicyclic Ring System
Contains a nitrogen atom
Application
Building block in organic synthesis
Pharmaceutical Potential
Antidepressant and anxiolytic drugs
Industrial and Scientific Use
Production of various materials
Check Digit Verification of cas no
The CAS Registry Mumber 1223573-40-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,5,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1223573-40:
(9*1)+(8*2)+(7*2)+(6*3)+(5*5)+(4*7)+(3*3)+(2*4)+(1*0)=127
127 % 10 = 7
So 1223573-40-7 is a valid CAS Registry Number.
1223573-40-7Relevant articles and documents
Synthesis and structural analysis of a new class of azaspiro[3.3]heptanes as building blocks for medicinal chemistry
Burkhard, Johannes A.,Guerot, Carine,Knust, Henner,Rogers-Evans, Mark,Carreira, Erick M.
supporting information; experimental part, p. 1944 - 1947 (2010/07/04)
Figure presented Straightforward access toward previously unreported substituted, heterocyclic spiro[3.3]heptanes is disclosed. These spirocyclic systems may be considered as alternatives to 1,3-heteroatom-substituted cyclohexanes, which are otherwise insufficiently stable to allow their use in drug discovery. Conformational details are discussed on the basis of X-ray crystallographic structures.
