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(1-(4-methoxybenzyl)-1H-1,2,4-triazol-5-yl)methanamine is a triazole derivative chemical compound characterized by a triazole ring, a methanamine group, and a 4-methoxybenzyl substituent. It has been investigated for its potential pharmaceutical properties, such as antifungal and antimicrobial activities, and may also be utilized in agricultural chemicals as a pesticide. The 4-methoxybenzyl group is believed to enhance its biological activities and pharmacokinetics, with ongoing research to explore its full spectrum of properties and applications.

199014-16-9

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199014-16-9 Usage

Uses

Used in Pharmaceutical Industry:
(1-(4-methoxybenzyl)-1H-1,2,4-triazol-5-yl)methanamine is used as an active pharmaceutical ingredient for its antifungal and antimicrobial properties, offering potential treatments for various infections caused by fungi and bacteria.
Used in Agricultural Chemicals Industry:
In the agricultural sector, (1-(4-methoxybenzyl)-1H-1,2,4-triazol-5-yl)methanamine is used as a potential pesticide, leveraging its antimicrobial properties to protect crops from harmful microorganisms and pests, thereby enhancing crop yield and quality.

Check Digit Verification of cas no

The CAS Registry Mumber 199014-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,0,1 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 199014-16:
(8*1)+(7*9)+(6*9)+(5*0)+(4*1)+(3*4)+(2*1)+(1*6)=149
149 % 10 = 9
So 199014-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N4O/c1-16-10-4-2-9(3-5-10)7-15-11(6-12)13-8-14-15/h2-5,8H,6-7,12H2,1H3

199014-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(4-methoxyphenyl)methyl]-1,2,4-triazol-3-yl]methanamine

1.2 Other means of identification

Product number -
Other names 5-(aminomethyl)-1-(4-methoxybenzyl)-1,2,4-triazole

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:199014-16-9 SDS

199014-16-9Relevant academic research and scientific papers

An efficient synthesis of 6-substituted 2-(2H-[1,2,4]triazol-3- ylmethyl)-1,2,3,4-tetrahydro-isoquinolines

Urban, Frank J.,Breitenbach, Ralph

, p. 645 - 653 (2007/10/03)

A synthesis of 6-nitro and 6-amino 2-(2H-[1,2,4]triazol-3- ylmethyl)1,2,3,4-tetrahydro-isoquinolines using a bis-alkylation process is described. 5-(Aminomethyl)-1-(p-methoxybenzyl)-triazole was prepared by a regioselective route from 1,2,4-triazole.

Tandem reduction studies of bromo compounds using tetrabutylammonium borohydride

Narasimhan,Swarnalakshmi,Balakumar,Velmathi

, p. 685 - 689 (2007/10/03)

Tetrabutylammonium borohydride can be used for multifunctional transformations through tandem reductions of halo compounds in THF.

Process and intermediates for preparing 4'-trifluoromethylbiphenyl-2-carboxylic acid [2-(2H-[1,2,4]triazol-3-ylmethyl)-1,2,3,4-tetrahydro-isoquinolin-6-yl]-a mide

-

, (2008/06/13)

A process for preparing the compound of formula (1) is disclosed. STR1 The starting materials are an N-triazolylmethyl-6-aminoisoquinoline and a 4-biphenyl-2-carboxylic acid derivative.

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