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5-HYDROXY-7-METHYL-1,3,4-TRIAZAINDOLIZINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5217-59-4

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5217-59-4 Usage

Chemical Family

Triazaindolizine derivatives

Structure

Heterocyclic compound with a ring structure containing nitrogen atoms

Molecular Weight

172.18 g/mol

Functional Groups

Hydroxyl group ( -\textOH ) attached to the 5th carbon atom
Methyl group ( -\textCH3 ) at the 7th carbon atom

Derived From

Indolizine

Potential Applications

Pharmaceutical research
Chemical research

Current Exploration

Properties and uses are still under investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 5217-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5217-59:
(6*5)+(5*2)+(4*1)+(3*7)+(2*5)+(1*9)=84
84 % 10 = 4
So 5217-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4O/c1-4-2-5(11)9-6-7-3-8-10(4)6/h2-3H,1H3,(H,7,8,9,11)

5217-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-3H-[1,2,4]triazolo[1,5-a]pyridin-5-one

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:5217-59-4 SDS

5217-59-4Downstream Products

5217-59-4Relevant academic research and scientific papers

Synthetic Versatility of β-Alkoxyvinyl Trichloromethyl Ketones for Obtaining [1,2,4]Triazolo[1,5- a ]pyrimidines

Souza, Laura A.,Santos, Josiane M.,Mittersteiner, Mateus,Andrade, Valquiria P.,Lobo, Marcio M.,Santos, Felipe B.,Bortoluzzi, Adailton J.,Bonacorso, Helio G.,Martins, Marcos A. P.,Zanatta, Nilo

, p. 3686 - 3695 (2018/07/21)

The synthetic versatility of 4-alkoxy-4-alkyl/aryl-1,1,1-trichloroalk-3-en-2-ones (enones) for the synthesis of [1,2,4]triazolo[1,5- a ]pyrimidines, in which the trichloromethyl group is either maintained or eliminated from the product by simply controlli

NMR determination of the structure of azolopyrimidines produced from reaction of bidentate electrophiles and aminoazoles

Hassaneen, Huwaida M. E.,Hassaneen, Hamdi M.,Khiry, Sherif F. M.,Pagni, Richard M.

experimental part, p. 217 - 222 (2008/10/09)

A variety of aminoazoles were reacted with bidentate electrophiles producing azolopyrimidines. The regioselectivity of the nucleophilic attack could be defined from the 13C chemical shift of the pyrimidine carbons and through NOE experiments.

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