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8-Benzyl-1,8-diazaspiro[4.5]decane is a unique chemical compound characterized by its spiro-structure that incorporates a benzyl group and a diaza ring. 8-BENZYL-1,8-DIAZASPIRO[4.5]DECANE is known for its potential chiral selectivity and has garnered interest in various scientific and industrial fields due to its diverse applications.

928034-30-4

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928034-30-4 Usage

Uses

Used in Coordination Chemistry:
8-Benzyl-1,8-diazaspiro[4.5]decane serves as a valuable ligand in coordination chemistry, playing a crucial role in the formation and stabilization of metal complexes. Its incorporation can influence the reactivity, selectivity, and properties of these complexes, making it an essential component in the design of new catalysts and materials.
Used in Organometallic Chemistry:
In organometallic chemistry, 8-benzyl-1,8-diazaspiro[4.5]decane is utilized for its ability to form stable complexes with metal centers. This feature is particularly useful in the development of homogeneous catalysts and the study of organometallic reaction mechanisms.
Used in Chiral Auxiliaries Synthesis:
8-BENZYL-1,8-DIAZASPIRO[4.5]DECANE has been employed in the synthesis of chiral auxiliaries, which are essential in asymmetric synthesis for inducing enantioselectivity in chemical reactions. Its unique structure contributes to the development of new methods for the production of enantiomerically pure compounds.
Used in Chromatography:
8-Benzyl-1,8-diazaspiro[4.5]decane has been utilized in the creation of chiral stationary phases for chromatography. These phases are vital for the separation of enantiomers, which is crucial in pharmaceutical development, as well as in the analysis and purification of chiral compounds.
Used in Pharmaceutical Development:
8-BENZYL-1,8-DIAZASPIRO[4.5]DECANE has been investigated for its potential pharmacological properties, including its use as an antipsychotic and anti-anxiety agent. Its unique structure and potential therapeutic effects make it a promising candidate for the development of new medications to treat various mental health disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 928034-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,0,3 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 928034-30:
(8*9)+(7*2)+(6*8)+(5*0)+(4*3)+(3*4)+(2*3)+(1*0)=164
164 % 10 = 4
So 928034-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N2/c1-2-5-14(6-3-1)13-17-11-8-15(9-12-17)7-4-10-16-15/h1-3,5-6,16H,4,7-13H2

928034-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Benzyl-1,8-diazaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names A-1912

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:928034-30-4 SDS

928034-30-4Relevant academic research and scientific papers

Construction of NH-Unprotected Spiropyrrolidines and Spiroisoindolines by [4+1] Cyclizations of γ-Azidoboronic Acids with Cyclic N-Sulfonylhydrazones

Cabal, María-Paz,López, Lucía,Valdés, Carlos

supporting information, (2021/12/09)

The reactions of N-sulfonylhydrazones derived from cyclic ketones with γ-azidopropylboronic acid and 2-(azidomethyl)phenylboronic acid give rise to spirocyclic pyrrolidines and spiroisoindolines, respectively. The reactions proceed without the need of any transition-metal catalyst through a domino process that comprises the formation of a Csp3-C and a Csp3-N bond of the former hydrazonic carbon. The scope of the reaction has been explored by the preparation of over 50 examples of NH-unprotected spirocyclic derivatives. Importantly, this methodology could be applied for the preparation of alkaloid steroids from steroid N-tosylhydrazones.

DIAZASPIRODECANE OREXIN RECEPTOR ANTAGONISTS

-

Page/Page column 27; 29, (2008/06/13)

The present invention is directed to diazaspirodecane compounds which are antagonists of orexin receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which orexin receptors are involved.

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