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Benzenamine, 4-(1H-1,2,3-triazol-4-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89221-20-5

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89221-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89221-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,2 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89221-20:
(7*8)+(6*9)+(5*2)+(4*2)+(3*1)+(2*2)+(1*0)=135
135 % 10 = 5
So 89221-20-5 is a valid CAS Registry Number.

89221-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2H-triazol-4-yl)aniline

1.2 Other means of identification

Product number -
Other names 1,2,3-triazole analogue,14

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:89221-20-5 SDS

89221-20-5Relevant academic research and scientific papers

BIFUNCTIONAL COMPOUNDS AND USE FOR REDUCING URIC ACID LEVELS

-

Paragraph 00141, (2016/12/22)

Bifunctional compounds that increase uric acid excretion and reduce uric acid production, and monofunctional compounds that either increase uric acid excretion or reduce uric acid production. Methods of using these compounds for reducing uric acid levels

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

-

, (2016/05/02)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.

NH-1,2,3-triazoles from azidomethyl pivalate and carbamates: Base-labile N-protecting groups

Loren, Jon C.,Krasiński, Antoni,Fokin, Valery V.,Sharpless, K. Barry

, p. 2847 - 2850 (2007/10/03)

NH-1,2,3-triazoles have been prepared via the copper(I)-catalyzed 1,3-dipolar cycloaddition between terminal alkynes and three N-protected organic azides, azidomethyl pivalate, azidomethyl morpholine-4-carboxylate, and azidomethyl N,N-diethylcarbarnate. T

Triazole compound and use thereof

-

, (2008/06/13)

A triazole compound or a pharmacologically acceptable salt thereof represented by the following formula (I) STR1 wherein R1 and R2 are the same or different from each other and each represents a hydrogen atom, a halogen atom or a Cs

Synthesis and in vitro antiinflammatory activity of 4-phenyl-1,2,3-triazole derivatives

Livi,Biagi,Ferretti,et al.

, p. 471 - 475 (2007/10/02)

This paper describes the preparation of new 4-phenyl-1,2,3-triazole derivatives of the general formulas I, II, and III, and their evaluation as in vitro prostaglandin synthesis inhibitors. These compounds generally inhibit the arachidonic acid-induced mal

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