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4-[3,5-Bis-(1-carbonylMethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-ylacetic acid is a complex chemical compound characterized by its molecular structure that incorporates multiple triazole and phenyl groups. 4-[3,5-Bis-(1-carbonylMethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-ylacetic acid is recognized as an azide-alkyne cycloaddition reagent, which is instrumental in bioconjugation and click chemistry reactions. Its potency and versatility stem from its capacity to create stable triazole linkages with a variety of other molecules. The inclusion of the acetic acid component further enhances its functionality and reactivity, positioning it as a beneficial asset in the realms of chemical synthesis and biomolecule modification. This multifaceted compound holds substantial promise for applications across pharmaceutical development, materials science, and bioengineering.

958299-25-7

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958299-25-7 Usage

Uses

Used in Pharmaceutical Development:
4-[3,5-Bis-(1-carbonylMethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-ylacetic acid serves as a key component in the synthesis of novel pharmaceuticals, leveraging its ability to form stable triazole linkages for creating diverse drug candidates.
Used in Materials Science:
In the field of materials science, {4-[3,5-Bis-(1-carbonylMethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-yl}- acetic acid acts as a valuable building block for the development of new materials with unique properties, thanks to its reactive and functional groups.
Used in Bioengineering:
4-[3,5-Bis-(1-carbonylMethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-ylacetic acid is utilized in bioengineering for its role in bioconjugation, allowing for the precise attachment of biologically active molecules to various surfaces or other biomolecules, which is crucial for the development of biosensors, drug delivery systems, and other biocompatible materials.
Used in Chemical Research and Development:
4-[3,5-Bis-(1-carbonylMethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-ylacetic acid is a vital tool in chemical research and development, providing a platform for the exploration of new chemical reactions, synthesis methods, and the modification of existing molecules to enhance their properties or create new functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 958299-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,2,9 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 958299-25:
(8*9)+(7*5)+(6*8)+(5*2)+(4*9)+(3*9)+(2*2)+(1*5)=237
237 % 10 = 7
So 958299-25-7 is a valid CAS Registry Number.

958299-25-7SDS

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 1H-1,2,3-Triazole-1-acetic acid, 4,4',4''-(1,3,5-benzenetriyl)tris-

1.2 Other means of identification

Product number -
Other names {4-[3,5-Bis-(1-carbonylmethyl-1H-[1,2,3]triazol-4-yl)-phenyl]-[1,2,3]triazol-1-yl}- acetic 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:958299-25-7 SDS

958299-25-7Upstream product

958299-25-7Downstream Products

958299-25-7Relevant academic research and scientific papers

An illustration of the limit of the metal organic framework's isoreticular principle using a semirigid tritopic linker obtained by "click" chemistry

Devic, Thomas,David, Olivier,Valls, Marion,Marrot, Jerome,Couty, Francois,Ferey, Gerard

, p. 12614 - 12615 (2007)

A new nitrogen-rich tricarboxylate linker was prepared by "click" chemistry and used for the preparation of a lanthanum-based open metal organic framework. This latter is built of inorganic 1-D rods connected through the tritopic linkers and illustrates o

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