Home Aldehydes 932-95-6
932-95-6,MFCD00216592
Catalog No.:AA003FYM

932-95-6 | 2,5-Thiophenedicarboxaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$16.00   $11.00
- +
1g
95%
in stock  
$26.00   $18.00
- +
5g
95%
in stock  
$128.00   $89.00
- +
  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003FYM
Chemical Name:
2,5-Thiophenedicarboxaldehyde
CAS Number:
932-95-6
Molecular Formula:
C6H4O2S
Molecular Weight:
140.1598
MDL Number:
MFCD00216592
SMILES:
O=Cc1ccc(s1)C=O
Properties
Properties
 
BP:
302°C at 760 mmHg  
Form:
Solid  
MP:
115-117 °C(lit.)  
Refractive Index:
1.5300 (estimate)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
110  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
1.2  

Literature

Title: (E)-1-Phenyl-2-({5-[(1E)-(2-phenyl-hydrazin-1-yl-idene)meth-yl]-2-thien-yl}methyl-idene)hydrazine.

Journal: Acta crystallographica. Section E, Structure reports online 20100301

Title: 2-[5-(Benzo[d]thia-zol-2-yl)thio-phen-2-yl]benzo[d]thia-zole.

Journal: Acta crystallographica. Section E, Structure reports online 20100301

Title: 5-{[(E)-2-(4-Iodo-phen-yl)hydrazinyl-idene]meth-yl}thio-phene-2-carbaldehyde.

Journal: Acta crystallographica. Section E, Structure reports online 20100201

Title: (E)-1-(3-Nitro-phen-yl)-2-({5-[(1E)-2-(3-nitro-phen-yl)hydrazin-1-ylidenemeth-yl]-2-thien-yl}methyl-idene)hydrazine.

Journal: Acta crystallographica. Section E, Structure reports online 20100201

Title: Synthesis of some thiophene, imidazole and pyridine derivatives exhibiting good anti-inflammatory and analgesic activities.

Journal: Medicinal chemistry (Shariqah (United Arab Emirates)) 20080301

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology 20050601

Title: Oxidation of heterocyclic and aromatic aldehydes to the corresponding carboxylic acids by Acetobacter and Serratia strains.

Journal: Biotechnology letters 20041101

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