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1048-17-5

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1048-17-5 Usage

Chemical structure

TASP is a bicyclic heterocycle with a spiro-ring structure containing a spiro nitrogen and oxygen atom.

Synonyms

TASP is also known as 1,3,8-Triazaspiro[4.5]decan-4-one,1-phenyl-8-(2-phenylethyl)-.

Synthesis

TASP is synthesized through a multistep reaction process.

Pharmaceuticals

Due to its unique spiro-ring structure, TASP can be a valuable building block for drug discovery and development.

Agrochemicals

TASP's structure also makes it potentially useful in the development of agrochemicals.

Ligand in metal-catalyzed reactions

TASP's properties may allow it to act as a ligand in metal-catalyzed reactions, which are important in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1048-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1048-17:
(6*1)+(5*0)+(4*4)+(3*8)+(2*1)+(1*7)=55
55 % 10 = 5
So 1048-17-5 is a valid CAS Registry Number.

1048-17-5SDS

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 8-phenethyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one

1.2 Other means of identification

Product number -
Other names 8-Phenethyl-4-phenyl-1-oxo-2,4,8-triazaspiro<4.5>decan

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:1048-17-5 SDS

1048-17-5Downstream Products

1048-17-5Relevant articles and documents

Discovery of N-(2-aryl-cyclohexyl) substituted spiropiperidines as a novel class of GlyT1 inhibitors

Pinard, Emmanuel,Ceccarelli, Simona M.,Stalder, Henri,Alberati, Daniela

, p. 349 - 353 (2007/10/03)

Screening of the Roche compound library led to the identification of cis-N-(2-phenyl-cyclohexyl)-spiropiperidine 1 as structurally novel GlyT1 inhibitor. The SAR, which was developed in this series, resulted in the discovery of highly potent compounds displaying excellent selectivity against the GlyT2 isoform.

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