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1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)is a chemical compound characterized by the molecular formula C10H8N4O2. It is a derivative of 1,2,4-triazole, featuring a carboxylic acid functional group and a phenylmethyl substituent. This versatile compound is known for its potential applications in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, as well as its potential biological activities, including antimicrobial and antifungal properties. It has also been explored for use in materials science and catalysis, showcasing its broad utility across different industries.

138624-97-2

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138624-97-2 Usage

Uses

Used in Pharmaceutical Synthesis:
1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)serves as a building block for the creation of novel agrochemicals, such as pesticides and herbicides, that can improve crop protection and yield.
Used in Organic Compounds Synthesis:
1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)is employed as a versatile synthetic building block in the preparation of various organic compounds, contributing to the advancement of organic chemistry and the development of new materials and molecules with specific properties.
Used in Antimicrobial and Anti-Fungal Applications:
1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)has been studied for its potential antimicrobial and antifungal properties, making it a candidate for use in applications that require the inhibition of microbial growth, such as in medical and industrial settings.
Used in Materials Science:
In the field of materials science, 1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)is explored for its potential to contribute to the development of new materials with unique properties, such as improved stability, reactivity, or selectivity.
Used in Catalysis:
1H-1,2,4-Triazole-3-carboxylic acid, 1-(phenylmethyl)has been investigated for its potential applications in catalysis, where it could be employed to enhance the efficiency of chemical reactions, leading to more sustainable and cost-effective processes in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 138624-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,2 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138624-97:
(8*1)+(7*3)+(6*8)+(5*6)+(4*2)+(3*4)+(2*9)+(1*7)=152
152 % 10 = 2
So 138624-97-2 is a valid CAS Registry Number.

138624-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1,2,4-triazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Benzyl-1H-1,2,4-triazole-3-carboxylic acid

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:138624-97-2 SDS

138624-97-2Downstream Products

138624-97-2Relevant academic research and scientific papers

INHIBITORS OF RECEPTOR INTERACTING PROTEIN KINASE I FOR THE TREATMENT OF DISEASE

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, (2021/03/13)

Disclosed herein are compounds which inhibit RIPK1, pharmaceutical compositions, and methods of treatment of RIPK1 -mediated diseases, such as neurodegenerative disorders, inflammatory disorders, and cancer.

Novel imidazole derivatives

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Page/Page column 16, (2009/01/23)

The invention is concerned with novel imidazole derivatives of formula (I), wherein m, E, R1, R2, R3, R4, R5, R6 and R7 are as defined in the description and in the claims, as we

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