1846-76-0,MFCD00016964
Catalog No.:AA003QBV

1846-76-0 | Ethyl coumarin-3-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$24.00   $17.00
- +
5g
>98.0%(GC)
in stock  
$66.00   $46.00
- +
25g
98%
in stock  
$138.00   $97.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003QBV
Chemical Name:
Ethyl coumarin-3-carboxylate
CAS Number:
1846-76-0
Molecular Formula:
C12H10O4
Molecular Weight:
218.2054
MDL Number:
MFCD00016964
SMILES:
CCOC(=O)c1cc2ccccc2oc1=O
NSC Number:
620
Properties
Properties
 
BP:
378°C at 760 mmHg  
Form:
Solid  
MP:
92-94°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
332  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.3  

Literature

Title: Photoinduced electron transfer in photorobust coumarins linked with electron donors affording long lifetimes of triplet charge-separated states.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry 20100823

Title: Effect of the synthetic coumarin, ethyl 2-oxo-2H-chromene-3-carboxylate, on activity of Crotalus durissus ruruima sPLA2 as well as on edema and platelet aggregation induced by this factor.

Journal: Toxicon : official journal of the International Society on Toxinology 20100701

Title: Ethyl 4-(2-fur-yl)-2-oxochroman-3-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20100601

Title: alpha-Glucosidase inhibitory antihyperglycemic activity of substituted chromenone derivatives.

Journal: Bioorganic & medicinal chemistry 20100101

Title: Biological activity of 3-formylchromones and related compounds.

Journal: In vivo (Athens, Greece) 20070101

Title: First total synthesis of (+/-)-Linderol A, a tricyclic hexahydrodibenzofuran constituent of Lindera umbellata bark, with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells.

Journal: The Journal of organic chemistry 20030221

Title: Wu C, et al. Solid-phase extraction of aflatoxins using a nanosorbent consisting of a magnetized nanoporous carbon core coated with a molecularly imprinted polymer. Mikrochim Acta. 2018 Oct 25;185(11):515.

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SDS
Tags:1846-76-0 Molecular Formula|1846-76-0 MDL|1846-76-0 SMILES|1846-76-0 Ethyl coumarin-3-carboxylate
Catalog No.: AA003QBV
1846-76-0,MFCD00016964
1846-76-0 | Ethyl coumarin-3-carboxylate
Pack Size: 1g
Purity: 98%
in stock
$24.00 $17.00
Pack Size: 5g
Purity: >98.0%(GC)
in stock
$66.00 $46.00
Pack Size: 25g
Purity: 98%
in stock
$138.00 $97.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA003QBV
Chemical Name: Ethyl coumarin-3-carboxylate
CAS Number: 1846-76-0
Molecular Formula: C12H10O4
Molecular Weight: 218.2054
MDL Number: MFCD00016964
SMILES: CCOC(=O)c1cc2ccccc2oc1=O
NSC Number: 620
Properties
BP: 378°C at 760 mmHg  
Form: Solid  
MP: 92-94°C  
Storage: Keep in dry area;2-8℃;  
Complexity: 332  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.3  
Literature fold

Title: Photoinduced electron transfer in photorobust coumarins linked with electron donors affording long lifetimes of triplet charge-separated states.

Journal: Chemphyschem : a European journal of chemical physics and physical chemistry20100823

Title: Effect of the synthetic coumarin, ethyl 2-oxo-2H-chromene-3-carboxylate, on activity of Crotalus durissus ruruima sPLA2 as well as on edema and platelet aggregation induced by this factor.

Journal: Toxicon : official journal of the International Society on Toxinology20100701

Title: Ethyl 4-(2-fur-yl)-2-oxochroman-3-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online20100601

Title: alpha-Glucosidase inhibitory antihyperglycemic activity of substituted chromenone derivatives.

Journal: Bioorganic & medicinal chemistry20100101

Title: Biological activity of 3-formylchromones and related compounds.

Journal: In vivo (Athens, Greece)20070101

Title: First total synthesis of (+/-)-Linderol A, a tricyclic hexahydrodibenzofuran constituent of Lindera umbellata bark, with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells.

Journal: The Journal of organic chemistry20030221

Title: Wu C, et al. Solid-phase extraction of aflatoxins using a nanosorbent consisting of a magnetized nanoporous carbon core coated with a molecularly imprinted polymer. Mikrochim Acta. 2018 Oct 25;185(11):515.

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