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1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE is a heterocyclic chemical compound with the molecular formula C3H3N3O. It features a five-membered ring structure composed of three nitrogen atoms and one oxygen atom. 1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE is widely recognized for its role as a building block in organic synthesis and pharmaceutical research, as well as its applications in the production of agrochemicals, specialty chemicals, dyes, pigments, and other fine chemicals. Its versatility and potential biological and pharmacological activities make it a valuable compound in various fields of chemistry and industry.

32829-25-7

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32829-25-7 Usage

Uses

Used in Organic Synthesis:
1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE is used as a key building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for the formation of diverse molecular architectures, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE serves as an essential component in the development of new drugs. Its derivatives have been investigated for their potential medicinal applications, including the treatment of various diseases and conditions.
Used in Agrochemical Production:
1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE is utilized in the production of agrochemicals, which are chemicals used in agriculture to enhance crop yield and protect plants from pests and diseases. Its incorporation into these products contributes to the development of effective and environmentally friendly agrochemicals.
Used in Specialty Chemicals:
1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE is also employed in the manufacture of specialty chemicals, which are high-value chemicals used in specific applications such as coatings, adhesives, and sealants. The unique properties of 1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE make it suitable for these specialized uses.
Used in Dyes and Pigments:
1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE is used in the preparation of dyes and pigments, which are essential for coloring various materials in industries such as textiles, plastics, and paints. Its presence in these products contributes to the development of vibrant and stable colorants.
Used in Fine Chemicals:
In the production of fine chemicals, 1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE plays a crucial role. Fine chemicals are high-purity chemicals used in various applications, including research, pharmaceuticals, and fragrances. 1H-[1,2,3]TRIAZOLE-4-CARBALDEHYDE's versatility and unique properties make it an indispensable component in the synthesis of these high-quality chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 32829-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,2 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32829-25:
(7*3)+(6*2)+(5*8)+(4*2)+(3*9)+(2*2)+(1*5)=117
117 % 10 = 7
So 32829-25-7 is a valid CAS Registry Number.

32829-25-7 Well-known Company Product Price

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  • Aldrich

  • (CBR00028)  1H-Indazol-1-ylacetic acid  AldrichCPR

  • 32829-25-7

  • CBR00028-1G

  • 1,611.09CNY

  • Detail

32829-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Indazol-1-ylacetic acid

1.2 Other means of identification

Product number -
Other names 2-indazol-1-ylacetic 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:32829-25-7 SDS

32829-25-7Relevant academic research and scientific papers

Synthesis and structural characterization of 1- and 2-substituted indazoles: Ester and carboxylic acid derivatives

Teixeira, Fatima C.,Ramos, Helene,Antunes, Ines F.,Curto, M. Joao M.,Duarte, M. Teresa,Bento, Isabel

, p. 867 - 889 (2006)

A series of indazoles substituted at the N-1 and N-2 positions with estercontaining side chains -(CH2)nCO2R of different lengths (n = 0-6, 9, 10) are described. Nucleophilic substitution reactions on halo esters (X(CH2)nCO2R) by 1H-indazole in alkaline solution lead to mixtures of N-1 and N-2 isomers, in which the N-1 isomer predominates. Basic hydrolysis of the ester derivatives allowed the synthesis of the corresponding indazole carboxylic acids. All compounds were fully characterised by multinuclear NMR and IR spectroscopies, MS spectrometry and elemental analysis; the NMR spectroscopic data were used for structural assignment of the N-1 and N-2 isomers. The molecular structure of indazol-2-yl-acetic acid (5b) was determined by X-ray diffraction, which shows a supramolecular architecture involving O2-H...N1 intermolecular hydrogen bonds.

COMPOUNDS USEFUL AS CSF1 MODULATORS

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Paragraph 00645; 00648; 00649, (2016/04/26)

This invention relates to novel compounds and to pharmaceutical compositions comprising the novel compounds. More specifically, the invention relates to compounds useful as Colony Stimulating Factor 1 Receptor (cFMS) modulators (e.g. cFMS inhibitors). This invention also relates to processes for preparing the compounds, uses of the compounds in treatment and methods of treatment employing the compounds. Specifically, the invention relates to the use of the compounds for the treatment of cancer and autoimmune diseases.

4-(Benzoimidazol-2-yl)-thiazole Compounds and Related Aza Derivatives

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Paragraph 0745; 0786, (2015/01/06)

The invention relates to compounds of Formula (I) wherein ring A, X, (R1)n, R2, R3, R4, R4′, R5, n, and p are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds as medicaments, especially as modulators of the CXCR3 receptor.

4-(BENZOIMIDAZOL-2-YL)-THIAZOLE COMPOUNDS AND RELATED AZA DERIVATIVES

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Page/Page column 97; 98; 106, (2013/08/15)

The invention relates to compounds of Formula (I) wherein ring A, X, (R1)n, R2, R3, R4, R4', R5, n, and p are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds as medicaments, especially as modulators of the CXCR3 receptor.

Ramoplanin derivatives possessing antibacterial activity

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Page/Page column 64, (2010/11/23)

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

Triterpene derivatives and endothelin-receptor antagonists containing the same

-

, (2008/06/13)

Triterpene derivatives of the formula (I): STR1 wherein R 1 is hydrogen or metabolic ester residue; and R 2 is hydrogen or --R 3 --R 4 wherein R 3 is --SO 3 --, --CH 2 COO--, --COCOO--, or --COR 5 COO-- (R 5 is lower alkylene or lower alkenylene), and R 4

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