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6-Benzyl-1,6-diazaspiro[3.4]octan-1-carboxylic acid tert-butyl ester is a complex chemical compound that features an ester derivative of 1,6-diazaspiro[3.4]octan-1-carboxylic acid with a benzyl group at the 6th position and a tert-butyl ester group. This unique molecular structure endows the compound with potential applications in pharmaceuticals and organic synthesis, which could contribute to the development of innovative drugs or materials. However, further research is necessary to explore its properties and uses comprehensively.

1148044-30-7

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1148044-30-7 Usage

Uses

Used in Pharmaceutical Industry:
6-Benzyl-1,6-diazaspiro[3.4]octan-1-carboxylic acid tert-butyl ester is used as a potential precursor in the synthesis of new pharmaceutical compounds due to its distinctive molecular structure. Its unique arrangement of atoms and functional groups may offer novel pathways for drug development, targeting specific biological processes or diseases.
Used in Organic Synthesis:
In the field of organic synthesis, 6-Benzyl-1,6-diazaspiro[3.4]octan-1-carboxylic acid tert-butyl ester serves as a versatile intermediate or building block for creating a variety of complex organic molecules. Its presence of a benzyl group and a tert-butyl ester group provides opportunities for further functionalization and modification, expanding the scope of organic chemistry.
Used in Research and Development:
6-Benzyl-1,6-diazaspiro[3.4]octan-1-carboxylic acid tert-butyl ester is utilized as a subject of study in research and development labs to understand its chemical properties, reactivity, and potential interactions with biological systems. This knowledge can inform the design of new experiments and the development of new applications for the compound.
While the specific applications of 6-Benzyl-1,6-diazaspiro[3.4]octan-1-carboxylic acid tert-butyl ester in different industries are not explicitly detailed in the provided materials, the general uses outlined above are inferred from its potential in pharmaceuticals, organic synthesis, and research, based on its unique molecular structure and properties. Further investigation would be required to pinpoint exact applications and industries where 6-Benzyl-1,6- diazaspiro[3.4]octan-1-carboxylic acid tert-butyl ester could be most beneficial.

Check Digit Verification of cas no

The CAS Registry Mumber 1148044-30-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,8,0,4 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1148044-30:
(9*1)+(8*1)+(7*4)+(6*8)+(5*0)+(4*4)+(3*4)+(2*3)+(1*0)=127
127 % 10 = 7
So 1148044-30-7 is a valid CAS Registry Number.

1148044-30-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 7-benzyl-1,7-diazaspiro[3.4]octane-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:1148044-30-7 SDS

1148044-30-7Relevant academic research and scientific papers

Preparation and characterization of N-(3-pyridinyl) spirocyclic diamines as ligands for nicotinic acetylcholine receptors

Sippy, Kevin B.,Anderson, David J.,Bunnelle, William H.,Hutchins, Charles W.,Schrimpf, Michael R.

scheme or table, p. 1682 - 1685 (2009/11/30)

Several N-pyridin-3-yl spirobicyclic diamines, designed as conformationally restricted analogs of tebanicline (ABT-594), were synthesized as novel ligands for nicotinic acetylcholine receptors (nAChR). The spirocyclic compounds exhibited weaker binding affinity, than other constrained analogs in accord with a pharmacophore model. Nevertheless, some (1a, 1b) possessed (partial) agonist potencies comparable to nicotine at the α4β2 subtype, but with greatly improved selectivity relative to the α3β4* nAChR.

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