Home Thiazoles 1826-11-5
1826-11-5,MFCD00272327
Catalog No.:AA0023XD

1826-11-5 | 2-Phenylthiazole

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1g
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$24.00   $17.00
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5g
95%
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$76.00   $54.00
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10g
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$119.00   $83.00
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25g
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0023XD
Chemical Name:
2-Phenylthiazole
CAS Number:
1826-11-5
Molecular Formula:
C9H7NS
Molecular Weight:
161.2236
MDL Number:
MFCD00272327
SMILES:
c1ccc(cc1)c1nccs1
Properties
Properties
 
BP:
277.4°C at 760 mmHg  
Form:
Solid  
MP:
114℃  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
121  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
2.6  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1937,vol.59,p.2262

[1]Patent:WO2006/123145,2006,A1,.Locationinpatent:Page/Pagecolumn68

[2]JournaloftheAmericanChemicalSociety,1937,vol.59,p.2262

[1]AngewandteChemie-InternationalEdition,2012,vol.51,#24,p.5971-5975

[2]ChemicalCommunications,2017,vol.53,#31,p.4339-4341

[3]Patent:JP2018/118935,2018,A,

Downstream Synthesis Route

[1]HelveticaChimicaActa,1947,vol.30,p.2058,2061

[1]Patent:WO2006/123145,2006,A1.Locationinpatent:Page/Pagecolumn68

[2]JournaloftheAmericanChemicalSociety,1937,vol.59,p.2262

[1]BulletindelaSocieteChimiquedeFrance,1967,p.4523-4533

[1]JournaloftheAmericanChemicalSociety,1994,vol.116,p.2292-2300

[1]Synthesis,2008,p.3099-3107

[2]Chemistry-AnAsianJournal,2015,vol.10,p.1725-1730

[3]Patent:US2005/101602,2005,A1.Locationinpatent:Page/Pagecolumn69

[4]Synlett,2007,p.2975-2978

[5]AngewandteChemie-InternationalEdition,2012,vol.51,p.5971-5975

[6]Patent:JP2018/118935,2018,A.Locationinpatent:Paragraph0074;0075

[7]TetrahedronLetters,2004,vol.45,p.7157-7161

[8]Chemistry-AEuropeanJournal,2017,vol.23,p.3743-3754

[9]ActaChemicaScandinavica,1992,vol.46,p.372-383

[10]Chemistry-AEuropeanJournal,2013,vol.19,p.16972-16980

[11]ChemicalCommunications,2016,vol.52,p.5171-5174

[12]ChemicalCommunications,2017,vol.53,p.4339-4341

Literature

Title: An investigation of phenylthiazole antiflaviviral agents.

Journal: Bioorganic & medicinal chemistry 20110615

Title: Bis(2-amino-1,3-benzothia-zol-3-ium) tetra-chloridozincate(II).

Journal: Acta crystallographica. Section E, Structure reports online 20110601

Title: Relating patenting and peer-review publications: an extended perspective on the vascular health and risk management literature.

Journal: Vascular health and risk management 20110101

Title: Synthesis and biological evaluation of 2-phenylthiazole-4-carboxamide derivatives as anticancer agents.

Journal: European journal of medicinal chemistry 20101101

Title: 1'-Acetyl-3-phenyl-6-oxa-4-thia-2-aza-spiro-[bicyclo-[3.2.0]hept-2-ene-7,3'-indolin]-2'-one.

Journal: Acta crystallographica. Section E, Structure reports online 20100901

Title: Design, synthesis, and structure-activity analysis of isoform-selective retinoic acid receptor beta ligands.

Journal: Journal of medicinal chemistry 20090326

Title: Indanylacetic acid derivatives carrying 4-thiazolyl-phenoxy tail groups, a new class of potent PPAR alpha/gamma/delta pan agonists: synthesis, structure-activity relationship, and in vivo efficacy.

Journal: Journal of medicinal chemistry 20070308

Title: Synthesis and biological evaluation of new thiazolyl/benzothiazolyl-amides, derivatives of 4-phenyl-piperazine.

Journal: Farmaco (Societa chimica italiana : 1989) 20050101

Title: Synthesis and structure-activity relationships of uracil derived human GnRH receptor antagonists: (R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5.

Journal: Bioorganic & medicinal chemistry letters 20041004

Title: Synthesis of potential aldose reductase inhibitors based on minimal pharmacophore requirements.

Journal: The Journal of pharmacy and pharmacology 20010601

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