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1-[1-(4-Methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-ethanone is a complex organic chemical compound characterized by the presence of a triazole ring, a 4-methoxy-benzyl group, and an ethanone moiety. The triazole ring, with its three nitrogen atoms, is recognized for its antifungal and antitumor properties, making it a valuable component in pharmaceutical chemistry. The 4-methoxy-benzyl group, featuring a methoxy substituent, is a common structural element in organic synthesis and contributes to the fragrance profile in perfumery. The ethanone group, a carbonyl component, is a fundamental part of ketones and plays a role in various biological metabolic pathways. 1-[1-(4-Methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-ethanone's unique structure and potential biological activities suggest it may find utility in both pharmaceutical and agrochemical sectors.

88860-93-9

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88860-93-9 Usage

Uses

Used in Pharmaceutical Industry:
1-[1-(4-Methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-ethanone is used as a pharmaceutical intermediate for its potential antifungal and antitumor properties. The triazole ring's bioactivity, combined with the versatility of the benzyl and ethanone groups, positions 1-[1-(4-Methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-ethanone as a candidate for the development of new drugs targeting fungal infections and cancer treatment.
Used in Agrochemical Industry:
In the agrochemical field, 1-[1-(4-Methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-ethanone is utilized as a starting material or intermediate in the synthesis of agrochemicals with antifungal properties. Its structural components can be tailored to create compounds that protect crops from fungal diseases, thereby increasing agricultural productivity.
Used in Perfumery:
1-[1-(4-Methoxy-benzyl)-1H-[1,2,3]triazol-4-yl]-ethanone is used as a fragrance ingredient in the perfumery industry. The 4-methoxy-benzyl group contributes a distinct scent profile, making it a valuable component in creating unique and complex fragrances for various applications, such as personal care products and scented goods.

Check Digit Verification of cas no

The CAS Registry Mumber 88860-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,6 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88860-93:
(7*8)+(6*8)+(5*8)+(4*6)+(3*0)+(2*9)+(1*3)=189
189 % 10 = 9
So 88860-93-9 is a valid CAS Registry Number.

88860-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[1-[(4-methoxyphenyl)methyl]triazol-4-yl]ethanone

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

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More Details:88860-93-9 SDS

88860-93-9Downstream Products

88860-93-9Relevant academic research and scientific papers

Hetero-Diels-Alder reactions of novel 3-triazolyl-nitrosoalkenes as an approach to functionalized 1,2,3-triazoles with antibacterial profile

Lopes, Susana M.M.,Novais, Juliana S.,Costa, Dora C.S.,Castro, Helena C.,Figueiredo, Agnes Marie S.,Ferreira, Vitor F.,Pinho e Melo, Teresa M.V.D.,da Silva, Fernando de Carvalho

, p. 1010 - 1020 (2017/12/15)

The generation and reactivity of 3-triazolyl-nitrosoalkenes are reported for the first time. The study showed that hetero-Diels-Alder reaction of these heterodienes is an interesting synthetic strategy to functionalized 1,2,3-triazoles, including 1,2,3-tr

REACTION OF 1-DIALKYLAMINO(ALKOXY)-1-BUTEN-3-ONES WITH SOME 1,3-DIPOLAR SYSTEMS

Markova, N. K.,Tsil'ko, A. E.,Galishev, V. A.,Maretina, I. A.

, p. 1990 - 1993 (2007/10/02)

The corresponding functionally substituted isoxazoles, pyrazoles, and triazoles were obtained by the reaction of 1-dialkylamino-1-buten-3-ones and 1-alkoxy-1-buten-3-ones with benzonitrile N-oxide, acetyl- and ethoxycarbonyl-N-phenylnitrile imines, and p-

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