155282-10-3 Usage
Explanation
Different sources of media describe the Explanation of 155282-10-3 differently. You can refer to the following data:
1. This compound has two interconnected rings, which are part of its molecular structure.
3. Diazabicyclic ring system
2. The compound contains a diazabicyclic ring, which is a type of ring structure with two nitrogen atoms and a specific arrangement of carbon atoms.
3. The compound has a methylene group, which is a single carbon atom bonded to two hydrogen atoms.
5. 7,7-Dimethyl substitution
6. Catalyst or ligand in organic and coordination chemistry
4. The compound is used to accelerate or facilitate chemical reactions without being consumed in the process. It can also act as a ligand, which is a molecule that binds to a central metal atom to form a coordination complex.
7. Facilitates various chemical reactions
5. The compound is known for its ability to help in a range of chemical reactions, such as ring-opening polymerization, addition reactions, and the preparation of chiral compounds.
8. Ring-opening polymerization of cyclic lactones
6. The compound can be used to initiate and control the polymerization of cyclic lactones, which are important in the synthesis of biodegradable polymers and pharmaceuticals.
9. Addition of silyl enol ethers to aldehydes
7. The compound can facilitate the reaction between silyl enol ethers and aldehydes, which is a key step in many organic synthesis processes.
10. Preparation of chiral epoxy alcohols
8. The compound can be used in the synthesis of chiral epoxy alcohols, which are important building blocks in the production of pharmaceuticals and other biologically active compounds.
11. Synthesis of pharmaceuticals and biologically active compounds
9. The compound is utilized in the development and production of various pharmaceuticals and compounds with biological activity, due to its versatile catalytic and ligand properties.
Methylene group
-CH2-
Check Digit Verification of cas no
The CAS Registry Mumber 155282-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 155282-10:
(8*1)+(7*5)+(6*5)+(5*2)+(4*8)+(3*2)+(2*1)+(1*0)=123
123 % 10 = 3
So 155282-10-3 is a valid CAS Registry Number.
155282-10-3Relevant articles and documents
Synthesis of bridged bicyclic hydrazines via endocyclic N-acylhydrazonium intermediates: A novel route to the 1-azatropane skeleton
Rutjes,Hiemstra,Pirrung,Speckamp
, p. 10027 - 10048 (2007/10/02)
Bicyclic molecules with the 1,7-diaza-6,6-dimethylbicyclo[2.2.1]heptane and 1,8-diaza-7,7-dimethylbicyclo[3.2.1]octane (1-aza-7,7-dimethytropane) skeleton are shown to be efficiently synthesized via cyclization reactions of endocyclic N-acylhydrazonium intermediates. By using a protected β-ketoester as the internal nucleophile, azacocaine analogues are also accessible via this methodology.
