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5052-95-9

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5052-95-9 Usage

General Description

1-Oxa-3,8-diazaspiro(4.5)decan 2-one is a chemical compound that belongs to the class of spiro compounds, which are characterized by a carbon atom linked to two different rings. It is a cyclic compound that contains a spiro nitrogen and oxygen atom. 1-Oxa-3,8-diazaspiro(4.5)decan 2-one has potential applications in pharmaceuticals, as it is structurally similar to some bioactive compounds and may have biological activity. Its spiro structure and oxygen-containing functional group make it an interesting target for synthesis and study in the field of medicinal chemistry. Additionally, its unique structure and potential biological activity make it a valuable compound for further research and potential drug development efforts.

Check Digit Verification of cas no

The CAS Registry Mumber 5052-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,5 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5052-95:
(6*5)+(5*0)+(4*5)+(3*2)+(2*9)+(1*5)=79
79 % 10 = 9
So 5052-95-9 is a valid CAS Registry Number.

5052-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oxa-3,8-diazaspiro[4.5]decan-2-one

1.2 Other means of identification

Product number -
Other names 1-oxa-3,8-diazaspiro<4.5>AGN-PC-00K8Q4

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:5052-95-9 SDS

5052-95-9Relevant articles and documents

Spirocyclic derivatives

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, (2016/04/09)

The present invention provides compounds of formula (I): compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease, disorder or condition ameliorated by inhibition of a dopamine transporter); and methods of treating patients with such compounds; wherein R1, R2, R3, R4, R5, R6, R9, R10, Q, X, Y, Z, A, L, B, m, n and p are as defined herein.

AUTOTAXIN INHIBITOR COMPOUNDS

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, (2015/04/15)

Described herein are compounds that are autotaxin inhibitors, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders associated with autotaxin activity.

Delayed and prolonged histone hyperacetylation with a selective HDAC1/HDAC2 inhibitor

Methot, Joey L.,Hoffman, Dawn Mampreian,Witter, David J.,Stanton, Matthew G.,Harrington, Paul,Hamblett, Christopher,Siliphaivanh, Phieng,Wilson, Kevin,Hubbs, Jed,Heidebrecht, Richard,Kral, Astrid M.,Ozerova, Nicole,Fleming, Judith C.,Wang, Hongmei,Szewczak, Alexander A.,Middleton, Richard E.,Hughes, Bethany,Cruz, Jonathan C.,Haines, Brian B.,Chenard, Melissa,Kenific, Candia M.,Harsch, Andreas,Secrist, J. Paul,Miller, Thomas A.

, p. 340 - 345 (2014/05/06)

The identification and in vitro and in vivo characterization of a potent SHI-1:2 are described. Kinetic analysis indicated that biaryl inhibitors exhibit slow binding kinetics in isolated HDAC1 and HDAC2 preparations. Delayed histone hyperacetylation and

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