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Home Amines 96-50-4
96-50-4,MFCD00005325
Catalog No.:AA00IJNF

96-50-4 | 2-Aminothiazole

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
98%
in stock  
$6.00   $4.00
- +
100g
98%
in stock  
$7.00   $5.00
- +
500g
98%
in stock  
$28.00   $20.00
- +
  • 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:
AA00IJNF
Chemical Name:
2-Aminothiazole
CAS Number:
96-50-4
Molecular Formula:
C3H4N2S
Molecular Weight:
100.1423
MDL Number:
MFCD00005325
SMILES:
N=c1scc[nH]1
Properties
Properties
 
BP:
117 °C (15.002 mmHg)  
Form:
Solid  
MP:
91-93 °C(lit.)  
Refractive Index:
1.5300 (estimate)  
Solubility:
1 M HCl: soluble50mg/mL, clear (dark yellow-brown)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
48.1  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.4  

Upstream Synthesis Route

[1]JournalfuerPraktischeChemie(Leipzig),1974,vol.316,p.349-352

[1]Patent:WO2008/33746,2008,A2,.Locationinpatent:Page/Pagecolumn56

[2]Patent:US5498630,1996,A,

[3]Patent:US2004/54186,2004,A1,.Locationinpatent:Page133

[1]Patent:US2002/161237,2002,A1,

[1]Synthesis,2012,vol.44,#7,p.1026-1029

[2]Patent:CN105348216,2016,A,.Locationinpatent:Paragraph0048;0049

[3]RecueildesTravauxChimiquesdesPays-Bas,1934,vol.53,p.77,78

[4]RecueildesTravauxChimiquesdesPays-Bas,1962,vol.81,p.554-564

[5]Patent:WO2016/55947,2016,A1,.Locationinpatent:Page/Pagecolumn142

[6]JournalofOrganicChemistry,2017,vol.82,#11,p.5947-5951

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,#33,p.13889-13895

Downstream Synthesis Route
96-50-4    590-92-1   
5,6-dihydro-thiazolo3,2-<i>a</i>pyrimidin-7-one;hydrobromide 

[1]JournaloftheAmericanChemicalSociety,1955,vol.77,p.117,119

[1]JournaloftheAmericanChemicalSociety,1949,vol.71,p.4007,4009

[1]Patent:CN107286150,2017,A.Locationinpatent:Paragraph0354;0355;0356

[2]JournaloftheAmericanChemicalSociety,2016,vol.138,p.14129-14137

[3]JournaloftheAmericanChemicalSociety,1946,vol.68,p.453,457

[4]RecueildesTravauxChimiquesdesPays-Bas,1954,vol.73,p.325,329

[5]Patent:US2537592,1945,

[6]SvenskKemiskTidskrift,1945,vol.57,p.229,232

[7]BulletindelaSocieteChimiquedeFrance,1962,p.2075-2078

[8]JournalofOrganicChemistry,2017,vol.82,p.5947-5951

[1]JournaloftheAmericanChemicalSociety,1955,vol.77,p.117,119

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1977,vol.15,p.850-852

Literature

Title: Gallardo-Godoy A, et al. 2-Aminothiazoles as therapeutic leads for prion diseases. J Med Chem. 2011 Feb 24;54(4):1010-21.

Title: Khalifa ME, et, al. Recent Developments and Biological Activities of 2-Aminothiazole Derivatives. Acta Chim Slov. 2018 Mar;65(1):1-22.

Title: Ran K, et, al. Identification of novel 2-aminothiazole conjugated nitrofuran as antitubercular and antibacterial agents. Bioorg Med Chem Lett. 2016 Aug 1;26(15):3669-74.

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SDS
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