5-Methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol

Base Information

• Chemical Name: 5-Methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol
• CAS No.: 35359-27-4
• Molecular Formula: C₁₁H₉N₃S
• Molecular Weight: 215.279
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID80351466
• Wikidata: Q82127902
• Mol file: 35359-27-4.mol

Synonyms:35359-27-4;5-Methyl-[1,2,4]triazolo[4,3-a]quinoline-1-thiol;5-methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol;5-methyl-2H-[1,2,4]triazolo[4,3-a]quinoline-1-thione;5-methyl[1,2,4]triazolo[4,3-a]quinoline-1(2H)-thione;Oprea1_461929;F1902-0023;SCHEMBL10577616;DTXSID80351466;MFCD01124519;STK965915;STL280121;AKOS000115878;AKOS002285172;CCG-309925;CS-0219071;EN300-02997;AB00714272-01;AF-399/36980034;SR-01000019036;SR-01000019036-1;Z56823197;F0239-0782;4-Methyl-1,2,4-triazolo[4,3-a]quinoline-1-thiol, 96%

Chemical Property of 5-Methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol

Chemical Property:

• Vapor Pressure: 0.000357mmHg at 25°C
• Melting Point: >250℃
• Refractive Index: 1.762
• Boiling Point: 318.6 °C at 760 mmHg
• Flash Point: 146.5 °C
• PSA: 68.99000
• Density: 1.41 g/cm³
• LogP: 2.47960
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 215.05171847
• Heavy Atom Count: 15
• Complexity: 372

Purity/Quality:

99% ^*data from raw suppliers

5-Methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol 95%+ ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC2=NNC(=S)N2C3=CC=CC=C13
• Uses: 5-Methyl-1H,2H-[1,2,4]triazolo[4,3-a]quinoline-1-thione is used as a reactant in the preparation of polyazaindenes and related compounds.

Technology Process of 5-Methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol

There total 3 articles about 5-Methyl[1,2,4]triazolo[4,3-a]quinoline-1-thiol 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:

→ 5-methyl-2H-[1,2,4]triazolo[4,3-a]quinoline-1-thione (35359-27-4)

Guidance literature:

at 180 ℃;

Reference yield:

2-hydrazinyl-4-methylquinoline (21703-52-6) → 5-methyl-2H-[1,2,4]triazolo[4,3-a]quinoline-1-thione (35359-27-4)

Guidance literature:

With pyridine;

Reference yield:

→ 5-Methyl-s-triazolo-<4,3-a>chinolin-1-thiol (35359-27-4)

Guidance literature:

2-Hydrazino-4-methylchinolin, Phenylisothiocyanat, Δ;

upstream raw materials:

2-hydrazinyl-4-methylquinoline

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