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1-phenyl-1H-imidazole-2-thiol

Base Information
  • Chemical Name:1-phenyl-1H-imidazole-2-thiol
  • CAS No.:17452-09-4
  • Molecular Formula:C9H8N2S
  • Molecular Weight:176.242
  • Hs Code.:2933290090
  • European Community (EC) Number:670-343-4
  • NSC Number:513730
  • DSSTox Substance ID:DTXSID50375139
  • Nikkaji Number:J68.949A
  • ChEMBL ID:CHEMBL309545
  • Mol file:17452-09-4.mol
1-phenyl-1H-imidazole-2-thiol

Synonyms:1-phenyl-1H-imidazole-2-thiol;17452-09-4;1-Phenyl-1H-imidazole-2(3H)-thione;1-Phenylimidazoline-2-thione;3-phenyl-1H-imidazole-2-thione;2-mercapto-1-phenylimidazole;1-Phenyl-1,3-dihydro-imidazole-2-thione;CHEMBL309545;2H-Imidazole-2-thione, 1,3-dihydro-1-phenyl-;1-phenylimidazole-2-thiol;1-Phenyl-1,3-dihydro-2H-imidazole-2-thione;NSC513730;SCHEMBL353826;DIISOBUTYLALUMINUMFLUORIDE;DTXSID50375139;BDBM50025497;MFCD00127929;STL124128;AKOS001429413;AKOS003406189;FS-1044;NSC 513730;NSC-513730;BB 0242511;CS-0244803;FT-0676324;1-phenyl-2,3-dihydro-1H-imidazole-2-thione;EN300-29457;2H-Imidazole-2-thione,1,3-dihydro-1-phenyl-;3J-919;1-Phenyl-1,3-dihydro-2H-imidazole-2-thione #;A811654;J-505058;F2147-0320;Z283822906

Suppliers and Price of 1-phenyl-1H-imidazole-2-thiol
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
  • TRC
  • 1-Phenyl-1H-imidazole-2-thiol
  • 50mg
  • $ 45.00
  • SynQuest Laboratories
  • 1-Phenylimidazoline-2-thione 98%
  • 5 g
  • $ 203.00
  • SynQuest Laboratories
  • 1-Phenylimidazoline-2-thione 98%
  • 1 g
  • $ 85.00
  • Matrix Scientific
  • 1-Phenyl-1H-imidazole-2-thiol 98%
  • 1g
  • $ 29.00
  • Matrix Scientific
  • 1-Phenyl-1H-imidazole-2-thiol 98%
  • 5g
  • $ 102.00
  • Crysdot
  • 1-Phenyl-1H-imidazole-2(3H)-thione 98%
  • 100g
  • $ 706.00
  • American Custom Chemicals Corporation
  • 1-PHENYL-2-IMIDAZOLIDINETHIONE 95.00%
  • 5MG
  • $ 505.87
  • AK Scientific
  • 1-Phenyl-1H-imidazole-2(3H)-thione
  • 1g
  • $ 83.00
Total 22 raw suppliers
Chemical Property of 1-phenyl-1H-imidazole-2-thiol
Chemical Property:
  • Vapor Pressure:0.00532mmHg at 25°C 
  • Melting Point:177 °C 
  • Refractive Index:1.727 
  • Boiling Point:274.7 °C at 760 mmHg 
  • PKA:11.78±0.50(Predicted) 
  • Flash Point:119.9 °C 
  • PSA:52.81000 
  • Density:1.31 g/cm3 
  • LogP:2.53490 
  • Storage Temp.:2-8°C 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:176.04081944
  • Heavy Atom Count:12
  • Complexity:207
Purity/Quality:

97% *data from raw suppliers

1-Phenyl-1H-imidazole-2-thiol *data from reagent suppliers

Safty Information:
  • Pictogram(s): R36/37/38:; 
  • Hazard Codes:R36/37/38:; 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)N2C=CNC2=S
  • General Description 1-Phenylimidazoline-2-thione is a heterocyclic compound featuring a phenyl group attached to the nitrogen of an imidazoline-2-thione scaffold. Its mass spectral fragmentation behavior is influenced by the N-phenyl substituent, which promotes hydrogen atom ejection from the phenyl ring, distinguishing it from alkyl-substituted analogs. Additionally, 1-PHENYLIMIDAZOLINE-2-THIONE has been studied in the context of enzyme inhibition, though specific details regarding its role as an inhibitor of human epithelial 15-lipoxygenase-2 (h15-LOX-2) remain unexplored in the provided abstracts.
Technology Process of 1-phenyl-1H-imidazole-2-thiol

There total 15 articles about 1-phenyl-1H-imidazole-2-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:
Guidance literature:
3-phenyl-2-thioxoimidazolidin-4-one; With sodium tetrahydroborate; lithium chloride; In 1,2-dimethoxyethane; ethanol; at -25 - -15 ℃; for 6h;
With hydrogenchloride; In 1,2-dimethoxyethane; ethanol; for 0.5h; Further stages.;
DOI:10.1055/s-2007-983740
Guidance literature:
With sulfuric acid;
Guidance literature:
Yield given. Multistep reaction;
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