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500024-85-1

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500024-85-1 Usage

Structure

A five-membered aromatic ring containing one nitrogen atom, with an N-hydroxy group and a carboximidamide functional group.

Type

A derivative of pyrrole

Classification

Hydroxamic acid

Applications

+ Chelating metal ions
+ Inhibiting histone deacetylases
+ Pharmaceutical agent (potential use in cancer treatment and other diseases)
+ Coordination chemistry
+ Catalyst in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 500024-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,0,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 500024-85:
(8*5)+(7*0)+(6*0)+(5*0)+(4*2)+(3*4)+(2*8)+(1*5)=81
81 % 10 = 1
So 500024-85-1 is a valid CAS Registry Number.

500024-85-1SDS

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 1H-Pyrrole-2-carboximidamide,N-hydroxy-

1.2 Other means of identification

Product number -
Other names N-hydroxy-1H-pyrrole-2-carboxamidine

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:500024-85-1 SDS

500024-85-1Upstream product

500024-85-1Relevant articles and documents

Synthesis of 2,4-Disubstituted Imidazoles via Nucleophilic Catalysis

Camp, Jason E.,Dunsford, Jay J.,Gill, Duncan M.,Ngwerume, Simbarashe,Saunders, Alexandra R.,Shabalin, Dmitrii A.

supporting information, p. 797 - 800 (2020/05/19)

A convergent, microwave-assisted protocol for the synthesis of disubstituted NH-imidazoles via nucleophilic catalysis is described. The substituted imidazoles are accessed via the intramolecular addition of a variety of amidoxime substrates to activated a

3,5-Disubstituted-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof

-

, (2008/06/13)

Disclosed are 3,5-disubstituted-[1,2,4]-oxadiazoles and analogs thereof, represented by the Formula I: wherein Ar1, R2, A, B and D are defined herein. The present invention relates to the discovery that compounds having Formula I are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention may be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

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