s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)-

Base Information

Chemical Name:s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)-
CAS No.:68869-49-8
Molecular Formula:C21H16ClN3OS
Molecular Weight:393.8892
Hs Code.:
DSSTox Substance ID:DTXSID10218957
ChEMBL ID:CHEMBL510458

Synonyms:s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)-;5-(4-Biphenoxymethyl)-1-(4-chlorophenyl)-1H-1,2,4-triazole-2-thiol;68869-49-8;CHEMBL510458;DTXSID10218957;LS-156116

Suppliers and Price of s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)-

Chemical Property:

Vapor Pressure:2.43E-12mmHg at 25°C
Boiling Point:554.6°C at 760 mmHg
Flash Point:289.2°C
Density:1.3g/cm³
XLogP3:5.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:393.0702610
Heavy Atom Count:27
Complexity:536

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=C(C=C2)OCC3=NNC(=S)N3C4=CC=C(C=C4)Cl

Technology Process of s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)-

There total 4 articles about s-Triazole-2-thiol, 5-(4-biphenoxymethyl)-1-(p-chlorophenyl)- 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: 85.0%

: 147865-11-0
N₁-[2-(biphenyl-4-yloxy)ethanoyl]-N₄-(4-chlorophenyl)-thiosemicarbazide

: 68869-49-8
5-[(biphenyl-4-yloxy)methyl]4-(4-chlorophenyl)-3-mercapto-(4H)-1,2,4-triazole

Guidance literature:: With triethylamine; In ethanol; Reflux;
DOI:10.1002/ardp.201100128

Reference yield:

: 92-69-3
4-Phenylphenol

: 68869-49-8
5-[(biphenyl-4-yloxy)methyl]4-(4-chlorophenyl)-3-mercapto-(4H)-1,2,4-triazole

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / acetone / Reflux

2: hydrazine hydrate / 4 h / Reflux

3: ethanol / Reflux

4: triethylamine / ethanol / Reflux

With potassium carbonate; hydrazine hydrate; triethylamine; In ethanol; acetone;
DOI:10.1002/ardp.201100128

Reference yield:

: 84161-08-0
2-(biphenyl-4-yloxy)acetic acid hydrazide

: 68869-49-8
5-[(biphenyl-4-yloxy)methyl]4-(4-chlorophenyl)-3-mercapto-(4H)-1,2,4-triazole

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / Reflux

2: triethylamine / ethanol / Reflux

With triethylamine; In ethanol;
DOI:10.1002/ardp.201100128