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1-[(AMinooxy)acetyl]-piperidine Monohydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

511531-59-2

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511531-59-2 Usage

Type

Chemical compound

Field of Use

Pharmaceuticals and research

Derivative of

Piperidine (a heterocyclic amine)

Contains

a. Aminooxy group
b. Acetyl group

Form

Monohydrochloride salt

Potential Applications

a. Anti-inflammatory agent
b. Anti-neurodegenerative agent
c. Treatment of diseases such as Alzheimer's and Parkinson's

Common Use

Reagent in chemical synthesis and organic reactions

Check Digit Verification of cas no

The CAS Registry Mumber 511531-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,5,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 511531-59:
(8*5)+(7*1)+(6*1)+(5*5)+(4*3)+(3*1)+(2*5)+(1*9)=112
112 % 10 = 2
So 511531-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O2.ClH/c8-11-6-7(10)9-4-2-1-3-5-9;/h1-6,8H2;1H

511531-59-2SDS

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 2-(aminooxy)-1-(piperidin-1-yl)ethanone hydrochloride

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

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

More Details:511531-59-2 SDS

511531-59-2Relevant academic research and scientific papers

POCHOXIME CONJUGATES USEFUL FOR THE TREATMENT OF HSP90 RELATED PATHOLOGIES

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Page/Page column 75, (2012/05/05)

The present invention includes novel derivatives, analogs, and intermediates of the natural products radicicol, pochonins, pochoximes, and their syntheses. The present invention also provides a pharamceutical composition comprising the present compound an

Asymmetric synthesis of pochonin e and F, revision of their proposed structure, and their conversion to potent Hsp90 inhibitors

Karthikeyan, Ganesan,Zambaldo, Claudio,Barluenga, Sofia,Zoete, Vincent,Karplus, Martin,Winssinger, Nicolas

supporting information; experimental part, p. 8978 - 8986 (2012/10/08)

A concise and modular synthesis of pochonin E and F, and their epimers at C-6 established the correct stereochemistry of these two natural products. Several members of the pochonin family have been shown to bind the heat shock protein 90 (Hsp90), which has been the focus of intense drug discovery efforts. Pochonin E and F as well as their epimers were derivatized into the corresponding pochoximes and further modified at the C-6 position. Molecular dynamics simulations, docking studies, and Hsp90 affinity measurements were performed to evaluate the impact of these modifications.

Synthesis of pochoxime prodrugs as potent HSP90 inhibitors

Wang, Cuihua,Barluenga, Sofia,Koripelly, Girish K.,Fontaine, Jean-Gonzague,Chen, Ruihong,Yu, Jin-Chen,Shen, Xiaodong,Chabala, John C.,Heck, James V.,Rubenstein, Allan,Winssinger, Nicolas

supporting information; experimental part, p. 3836 - 3840 (2010/04/05)

Pochoximes are potent inhibitors of heat shock protein 90 (HSP90) based on the radicicol pharmacophores. Herein we present a pharmacokinetics and pharmacodynamics evaluation of this compound series as well as a phosphate prodrug strategy to facilitate for

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