Home Pyridines 14294-11-2
14294-11-2,MFCD00041227
Catalog No.:AA003B6X

14294-11-2 | 1-(Pyridin-2-yl)thiourea

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1g
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5g
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10g
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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:
AA003B6X
Chemical Name:
1-(Pyridin-2-yl)thiourea
CAS Number:
14294-11-2
Molecular Formula:
C6H7N3S
Molecular Weight:
153.2049
MDL Number:
MFCD00041227
SMILES:
NC(=S)Nc1ccccn1
NSC Number:
176341
Properties
Properties
 
Form:
Solid  
MP:
148-150°C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
126  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
0.6  

Upstream Synthesis Route

[1]Synthesis,1988,#6,p.456-459

[2]BioorganicandMedicinalChemistryLetters,2006,vol.16,#14,p.3706-3712

[3]BioorganicandMedicinalChemistryLetters,2008,vol.18,#2,p.634-639

[4]JournaloftheChemicalSociety,1955,p.803

[5]JournalofOrganicChemistryUSSR(EnglishTranslation),1991,vol.27,#1.2,p.177-182

[6]ZhurnalOrganicheskoiKhimii,1991,vol.27,#1,p.201-206

[7]ZeitschriftfuerNaturforschung,TeilB:AnorganischeChemie,OrganischeChemie,1986,vol.41,#1,p.101-104

[8]JournalofMedicinalChemistry,1997,vol.40,#12,p.1901-1905

[9]BioorganicandMedicinalChemistryLetters,2003,vol.13,#16,p.2641-2645

[10]EuropeanJournalofMedicinalChemistry,2003,vol.38,#3,p.313-318

[11]Phosphorus,SulfurandSiliconandtheRelatedElements,2006,vol.181,#6,p.1381-1389

[12]BioorganicandMedicinalChemistryLetters,2005,vol.15,#12,p.3081-3085

[13]HeteroatomChemistry,2009,vol.20,#7,p.418-424

[14]Patent:US7105508,2006,B1,.Locationinpatent:Page/Pagecolumn75

[15]BioorganicandMedicinalChemistry,2013,vol.21,#21,p.6385-6397

[16]MedChemComm,2016,vol.7,#9,p.1768-1774

[17]Patent:WO2018/89261,2018,A2,.Locationinpatent:Paragraph0893;0896;0897

[1]EuropeanJournalofMedicinalChemistry,2016,vol.119,p.83-95

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,2006,vol.181,#7,p.1665-1673

[2]NewJournalofChemistry,2018,vol.42,#15,p.12649-12665

[3]EuropeanJournalofMedicinalChemistry,2004,vol.39,#10,p.867-872

[4]EuropeanJournalofMedicinalChemistry,2008,vol.43,#4,p.749-754

[5]EuropeanJournalofMedicinalChemistry,2009,vol.44,#3,p.1100-1105

[1]JournaloftheChemicalSociety,1955,p.803

[2]JournalofMedicinalChemistry,2011,vol.54,#4,p.1010-1021

[3]BioorganicandMedicinalChemistry,2013,vol.21,#21,p.6385-6397

[4]EuropeanJournalofMedicinalChemistry,2016,vol.119,p.83-95

[5]MedChemComm,2016,vol.7,#9,p.1768-1774

[6]Patent:WO2018/89261,2018,A2,

[1]JournalofMedicinalChemistry,2011,vol.54,#4,p.1010-1021

Downstream Synthesis Route

[1]CollectionofCzechoslovakChemicalCommunications,1982,vol.47,p.877-883

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1987,vol.26,p.856-860

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1981,vol.20,p.683-685

[1]JournaloftheIndianChemicalSociety,1991,vol.68,p.171-172

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1981,vol.20,p.683-685

Literature

Title: Thiourea-based non-nucleoside inhibitors of HIV reverse transcriptase as bifunctional organocatalysts in the asymmetric Strecker synthesis.

Journal: Bioorganic & medicinal chemistry 20051001

Title: Substituted heterocyclic thiourea compounds as a new class of anti-allergic agents inhibiting IgE/Fc epsilon RI receptor mediated mast cell leukotriene release.

Journal: Bioorganic & medicinal chemistry 20030320

Title: Inhibition of mast cell leukotriene release by thiourea derivatives.

Journal: Bioorganic & medicinal chemistry letters 20030210

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