1H-1,2,3-Triazole-4-carboxaldehyde, 1-(4-methylphenyl)-

Base Information

• Chemical Name: 1H-1,2,3-Triazole-4-carboxaldehyde, 1-(4-methylphenyl)-
• CAS No.: 113934-25-1
• Molecular Formula: C10H9N3O
• Molecular Weight: 187.201
• DSSTox Substance ID: DTXSID50447204
• Wikidata: Q82266030
• ChEMBL ID: CHEMBL1823301
• Mol file: 113934-25-1.mol

Synonyms:1-(4-methylphenyl)-1H-1,2,3-triazole-4-carbaldehyde;MePh-TCHO

Chemical Property of 1H-1,2,3-Triazole-4-carboxaldehyde, 1-(4-methylphenyl)-

Chemical Property:

• XLogP3: 1.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 187.074561919
• Heavy Atom Count: 14
• Complexity: 202

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)N2C=C(N=N2)C=O

Technology Process of 1H-1,2,3-Triazole-4-carboxaldehyde, 1-(4-methylphenyl)-

There total 12 articles about 1H-1,2,3-Triazole-4-carboxaldehyde, 1-(4-methylphenyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

Propiolaldehyde diethyl acetal (10160-87-9) + p-methylazidobenzene (2101-86-2) → 1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxaldehyde (113934-25-1)

Guidance literature:

With copper(II) sulfate; sodium L-ascorbate; In water; tert-butyl alcohol; at 70 ℃; for 24h; Solvent;

DOI:10.1016/j.tetlet.2017.10.023

Reference yield: 86.0%

2-diazo-malonaldehyde (50704-41-1) + p-toluidine hydrochloride (540-23-8) → 1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxaldehyde (113934-25-1)

Guidance literature:

In water; at 20 ℃; for 24h;

DOI:10.1016/j.bmc.2006.08.019

Reference yield: 86.0%

→ 1-(4-methylphenyl)-1H-1,2,3-triazole-4-carboxaldehyde (113934-25-1)

Guidance literature:

upstream raw materials:

2-diazo-malonaldehyde

p-toluidine hydrochloride

p-methylazidobenzene

1‐(4‐methylphenyl)‐1H‐1,2,3‐triazole‐4‐yl‐methanol