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162045-53-6

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  • SAGECHEM/tert-Butyl 4-(2-oxobenzo[d]oxazol-3(2H)-yl)piperidine-1-carboxylate/SAGECHEM/Manufacturer in China

    Cas No: 162045-53-6

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162045-53-6 Usage

General Description

Tert-butyl 4-(2-oxobenzo[d]oxazol-3(2H)-yl)piperidine-1-carboxylate is a complex chemical compound with a molecular formula C19H23N3O4. It is a piperidine derivative containing a benzooxazole moiety. This chemical is often used in scientific research and drug development due to its potential biological activity. Its unique structure and hydrophobic properties make it a valuable tool in the study of biological systems, particularly in the field of medicinal chemistry. Additionally, this compound may have potential applications in the development of new pharmaceuticals and other bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 162045-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,4 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162045-53:
(8*1)+(7*6)+(6*2)+(5*0)+(4*4)+(3*5)+(2*5)+(1*3)=106
106 % 10 = 6
So 162045-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H22N2O4/c1-17(2,3)23-15(20)18-10-8-12(9-11-18)19-13-6-4-5-7-14(13)22-16(19)21/h4-7,12H,8-11H2,1-3H3

162045-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(2-oxo-1,3-benzoxazol-3-yl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names Y6073

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:162045-53-6 SDS

162045-53-6Relevant articles and documents

Effects of Pimozide Derivatives on pSTAT5 in K562 Cells

Rondanin, Riccardo,Simoni, Daniele,Maccesi, Martina,Romagnoli, Romeo,Grimaudo, Stefania,Pipitone, Rosaria Maria,Meli, Maria,Cascio, Antonio,Tolomeo, Manlio

, p. 1183 - 1190 (2017)

STAT5 is a transcription factor, a member of the STAT family of signaling proteins. STAT5 is involved in many types of cancer, including chronic myelogenous leukemia (CML), in which this protein is found constitutively activated as a consequence of BCR-ABL expression. The neuroleptic drug pimozide was recently reported to act as an inhibitor of STAT5 phosphorylation and is capable of inducing apoptosis in CML cells in vitro. Our research group has synthesized simple derivatives of pimozide with cytotoxic activity and that are able to decrease the levels of phosphorylated STAT5. In this work we continued the search for novel STAT5 inhibitors, synthesizing compounds in which the benzoimidazolinone ring of pimozide is either maintained or modified, in order to obtain further structure–activity relationship information for this class of STAT5 inhibitors. Two compounds of the series showed potent cytotoxic activity against BCR-ABL-positive and pSTAT5-overexpressing K562 cells and were able to markedly decrease the levels of phosphorylated STAT5.

Method for treating allergies using substituted pyrazoles

-

, (2008/06/13)

A method for treating an allergic condition, including an atopic allergic condition, using substituted pyrazoles.

Design and synthesis of N-alkylated saccharins as selective α-1a adrenergic receptor antagonists

Nerenberg, Jennie B.,Erb, Jill M.,Thompson, Wayne J.,Lee, Hee-Yoon,Guare, James P.,Munson, Peter M.,Bergman, Jeffrey M.,Huff, Joel R.,Broten, Theodore P.,Chang, Raymond S. L.,Chen, Tsing B.,O'Malley, Stacey,Schorn, Terry W.,Scott, Ann L.

, p. 2467 - 2472 (2007/10/03)

Benign prostatic hyperplasia can be managed pharmacologically with α-1 adrenergic receptor antagonists. Agents that demonstrate selectivity for the α-la receptor subtype may offer advantages in clinical applications with respect to hypotensive side effect

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