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3973-08-8,MFCD00623589
Catalog No.:AA003LZP

3973-08-8 | Thiazole-4-carboxylic acid

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1g
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$8.00   $6.00
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5g
98%
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$19.00   $14.00
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25g
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$37.00   $26.00
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100g
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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:
AA003LZP
Chemical Name:
Thiazole-4-carboxylic acid
CAS Number:
3973-08-8
Molecular Formula:
C4H3NO2S
Molecular Weight:
129.1371
MDL Number:
MFCD00623589
SMILES:
OC(=O)c1cscn1
NSC Number:
195467
Properties
Properties
 
BP:
319.2°C at 760 mmHg  
Form:
Solid  
MP:
195-199 °C(lit.);  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
106  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.8  

Upstream Synthesis Route

[1]Patent:WO2006/46031,2006,A1,.Locationinpatent:Page/Pagecolumn85-86

[2]Patent:WO2007/122410,2007,A1,.Locationinpatent:Page/Pagecolumn97

[1]OrganicLetters,2011,vol.13,#19,p.5358-5361

[1]AngewandteChemie,1992,vol.104,#6,p.748-749

[2]Patent:CN104557902,2018,B,.Locationinpatent:Paragraph0063;0076;0081;0088;0089;0102

[1]Patent:CN107417639,2017,A,.Locationinpatent:Paragraph0023;0029;0030;0031;0032;0033;0034-0041

[1]JournalofMedicinalChemistry,2006,vol.49,#2,p.511-522

Downstream Synthesis Route

[1]HelveticaChimicaActa,1942,vol.25,p.1075

[1]JournaloftheChemicalSociety,1957,p.689,696

[1]JournaloftheChemicalSociety,1957,p.689,696

[1]JournaloftheChemicalSociety,1957,p.689,696

[1]HelveticaChimicaActa,1937,vol.20,p.204

Literature

Title: Mechanism selection for regiocontrol in base-assisted, palladium-catalysed direct C-H coupling with halides: first approach for oxazole- and thiazole-4-carboxylates.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20111216

Title: Design, synthesis, and evaluation of alpha-ketoheterocycles as class C beta-lactamase inhibitors.

Journal: Bioorganic & medicinal chemistry 20010801

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