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155282-10-3

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155282-10-3 Usage

Explanation

This compound has two interconnected rings, which are part of its molecular structure.
3. Diazabicyclic ring system

Explanation

The compound contains a diazabicyclic ring, which is a type of ring structure with two nitrogen atoms and a specific arrangement of carbon atoms.

Explanation

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

Explanation

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

Explanation

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

Explanation

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

Explanation

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

Explanation

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

Explanation

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.

155282-10-3Downstream Products

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.

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