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(1-Ethyl-1H-1,2,4-triazol-5-yl)methanol, a chemical compound with the molecular formula C6H10N2O, is a derivative of triazole, characterized by a five-membered ring structure containing three nitrogen atoms and two carbon atoms. This versatile compound is recognized for its potential applications in various fields, particularly in pharmaceuticals and agriculture, where it serves as a building block for drug synthesis and a fungicide, respectively. Additionally, it is utilized in research and development as a reagent in organic synthesis, highlighting its significance in scientific exploration.

215868-81-8

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215868-81-8 Usage

Uses

Used in Pharmaceutical Industry:
(1-Ethyl-1H-1,2,4-triazol-5-yl)methanol is used as a building block for the synthesis of pharmaceutical drugs. Its unique chemical structure allows it to be incorporated into various drug molecules, potentially enhancing their therapeutic properties and effectiveness in treating different medical conditions.
Used in Agricultural Industry:
In agriculture, (1-Ethyl-1H-1,2,4-triazol-5-yl)methanol is used as a fungicide to protect crops from fungal infections. Its ability to inhibit fungal growth contributes to maintaining crop health and improving yield, ensuring a stable food supply.
Used in Research and Development:
(1-Ethyl-1H-1,2,4-triazol-5-yl)methanol is utilized as a reagent in organic synthesis within research and development. Its chemical properties make it a valuable component in the creation of new compounds and materials, driving scientific innovation and discovery.
While the compound may possess potential medicinal and biological properties, further research is necessary to fully understand its effects and applications, paving the way for future advancements in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 215868-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,8,6 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 215868-81:
(8*2)+(7*1)+(6*5)+(5*8)+(4*6)+(3*8)+(2*8)+(1*1)=158
158 % 10 = 8
So 215868-81-8 is a valid CAS Registry Number.

215868-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-ethyl-1,2,4-triazol-3-yl)methanol

1.2 Other means of identification

Product number -
Other names QC-774

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:215868-81-8 SDS

215868-81-8Relevant articles and documents

DEUTERIUM-MODIFIED TRIAZOLO-PYRIDAZINE DERIVATIVES AS GABA-A RECEPTOR MODULATORS

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Page/Page column 32, (2011/02/24)

This invention relates to deuterated substituted triazolo-pyridazines and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering an αl-GABAA receptor antagonist or an α2- and/or an α3-GABAA receptor partial agonist.

NOVEL HERBICIDES

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Page/Page column 53, (2008/12/06)

The present invention relates to novel compounds of formula (I): wherein R1, R2, R3, R4, m, R5, R6, n and Y are as defined in claim 1; or N-oxides, salts and optical isomers thereof. Furthermore, the present invention relates to processes for preparing compounds of formula (I), to intermediates used in the preparation of compounds of formula (I), to herbicidal compositions comprising compounds of formula (I) and to methods of using compounds of formula (I) to control plants or to inhibit plant growth.

7-(1,1-Dimethylethyl)-6-(2-ethyl-2H-1,2,4-triazol-3-ylmethoxy) -3-(2-fluorophenyl)-1,2,4-triazolo[4,3-b]pyridazine: A functionally selective γ-aminobutyric acidA (GABAA) α2/α3- subtype selective agonist that exhibits potent anxiolyti

Carling, Robert W.,Madin, Andrew,Guiblin, Alec,Russell, Michael G. N.,Moore, Kevin W.,Mitchinson, Andrew,Sohal, Bindi,Pike, Andrew,Cook, Susan M.,Ragan, Ian C.,McKernan, Ruth M.,Quirk, Kathleen,Ferris, Pushpinder,Marshall, George,Thompson, Sally Ann,Wafford, Keith A.,Dawson, Gerard R.,Atack, John R.,Harrison, Timothy,Castro, José L.,Street, Leslie J.

, p. 7089 - 7092 (2007/10/03)

There is increasing evidence that compounds with selectivity for γ-aminobutyric acidA (GABAA) α2- and/or α3-subtypes may retain the desirable anxiolytic activity of nonselective benzodiazepines but possess an improved side effect pro

Substituted triazolo-pyridazine derivative, pharmaceutical compositions made therefrom

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, (2008/06/13)

7-(1,1 -Dimethylethyl)-6-(2-ethyl-2H-1,2,4-triazol-3-ylmethoxy)-3-(2-fluorophenyl)-1,2,4-triazolo[4,3-b]pyridazine, and pharmaceutically acceptable salts thereof are selective ligands for GABAAreceptors useful in the treatment of disorders of t

Substituted 1,2,4-triazolo[3,4-a]phthalazine derivatives as GABA alpha 5 ligands

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, (2008/06/13)

Substituted 1,2,4-Triazolo[3,4-A]phthalazine derivatives are GABA Alpha 5 ligands and are represented by the formula

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