Chemodex

8-Methoxychromone-3-carboxylic acid

Product Code:
 
CDX-M0836
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
Short term: +20°C. Long term: +20°C
1 / 1
Chemical Structure

Chemical Structure

No additional charges, what you see is what you pay! *

CodeSizePrice
CDX-M0836-G0011 g£156.00
Quantity:
CDX-M0836-G0055 g£591.00
Quantity:
Prices exclude any Taxes / VAT
Stay in control of your spending. These prices have no additional charges to UK mainland customers, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: Switzerland.
Typical lead time: 7-10 working days.
Contact us for more accurate information.
  • Further Information
  • Documents
  • References
  • Show All

Further Information

Appearance:
Solid.
CAS:
2555-20-6
Description:
8-Methoxychromone-3-carboxylic acid is a substituted chromone/coumarin derivative. It is used in organic synthesis for building heterocyclic compounds, biological active substances, dyes or fluorescent probes.
EClass:
32160000
Form:
solid
GHS Symbol:
GHS07
Handling Advice:
Protect from light and moisture.
Hazards:
H315-H319-H335
InChi:
InChI=1S/C11H8O5/c1-15-8-4-2-3-6-5-7(10(12)13)11(14)16-9(6)8/h2-5H,1H3,(H,12,13)
InChiKey:
SFAPWVZFUHJZIC-UHFFFAOYSA-N
MDL:
MFCD01116499
Molecular Formula:
C11H8O5
Molecular Weight:
220.18
Package Type:
Vial
Precautions:
P280-P261-P304-P340-P302-P352-P362+P364-P305-P351-P338
Signal word:
Warning
SMILES:
COC1=CC=CC2=C1OC(=O)C(=C2)C(=O)O
Solubility Chemicals:
Soluble in DMSO, DMF or acetonitrile.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at RT.

Documents

References

(1) K.V. Masrani, et al.; J. Appl. Chem. Biotechnol. 24, 331 (1974) | (2) J.L. Scott & C.L. Raston; Green Chem. 2, 245 (2000) | (3) A.H. Rezayan, et al.; Chem. Biol. Drug Design 80, 929 (2012) | (4) M. Saeedi, et al.; Bioorg. Chem. 70, 86 (2017) | (5) T. Abdizadeh, et al.; Eur. J. Med. Chem. 132, 42 (2017)