Home Other Building Blocks 90-33-5
90-33-5,MFCD00270380
Catalog No.:AA006RJT

90-33-5 | 7-Hydroxy-4-methylcoumarin

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
99%
in stock  
$7.00   $5.00
- +
25g
99%
in stock  
$9.00   $7.00
- +
100g
99%
in stock  
$24.00   $17.00
- +
500g
99%
in stock  
$86.00   $61.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA006RJT
Chemical Name:
7-Hydroxy-4-methylcoumarin
CAS Number:
90-33-5
Molecular Formula:
C10H8O3
Molecular Weight:
176.1687
MDL Number:
MFCD00270380
SMILES:
Oc1ccc2c(c1)oc(=O)cc2C
Properties
Properties
 
BP:
267.77°C (rough estimate)  
Form:
Solid  
MP:
188.5-190 °C(lit.)  
Refractive Index:
1.5036 (estimate)  
Solubility:
Solubility Practically insoluble in water; slightly soluble in ethanol, ether,chloroform; soluble inmethanol  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
257  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
1.9  

Literature

Title: García-Vilas JA, et al. 4-methylumbelliferone inhibits angiogenesis in vitro and in vivo. J Agric Food Chem. 2013 May 1;61(17):4063-71.

Application
4-Methylumbelliferone is a key compound widely utilized in the synthesis of various medicinal compounds and fluorescent probes. It serves as a foundational component for the creation of diverse molecules with pharmaceutical and diagnostic applications. Specifically, it is employed in the production of coumarin triazole derivatives, which hold promise as antimicrobial agents, and coumarin salen-based fluorescence sensors used for detecting Mg2+. Additionally, it plays a crucial role in the synthesis of pyranocoumarin derivatives, which exhibit potential as anti-hyperglycemic and anti-dyslipidemic agents, as well as coumarin piperazine derivatives, which are being explored as potential multireceptor atypical antipsychotics. Moreover, 4-Methylumbelliferone is essential in the creation of 4-methylumbelliferyl T-antigen, a substrate utilized in enzymatic assays for endo-α-N-acetylgalactosaminidase. Overall, 4-Methylumbelliferone serves as a versatile building block in the realm of medicinal chemistry and diagnostics, enabling the development of novel therapeutic and diagnostic agents.
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SDS
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