7-Methoxycoumarin-4-acetic acid
| Code | Size | Price |
|---|
| CDX-M0028-M500 | 500 mg | £121.00 |
Quantity:
| CDX-M0028-G001 | 1 g | £194.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
MCA; 7-MeO-Coumarin-AcOH; 7-Methoxy-2-oxo-2H-1-benzopyran-4-acetic acid; NSC 378137
Appearance:
White powder.
CAS:
62935-72-2
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C12H10O5/c1-16-8-2-3-9-7(4-11(13)14)5-12(15)17-10(9)6-8/h2-3,5-6H,4H2,1H3,(H,13,14)
InChiKey:
ZEKAXIFHLIITGV-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 62935-72-2. Formula: C12H10O5. MW: 234.2. Synthetic Florescent probe that is commonly used as a building block to synthesize coumarin-type fluorescent probes. Spectral data: lambdaex 320 nm, lambdaem 380 nm in methanol. It is used as a fluorescent label for peptides. It is widely used for developing FRET peptide substrates for analyzing protease activities and for HPLC derivatization by fluorescence detection.
MDL:
MFCD00009774
Molecular Formula:
C12H10O5
Molecular Weight:
234.2
Package Type:
Vial
Product Description:
Florescent probe that is commonly used as a building block to synthesize coumarin-type fluorescent probes. Spectral data: lambdaex 320 nm, lambdaem 380 nm in methanol. It is used as a fluorescent label for peptides. It is widely used for developing FRET peptide substrates for analyzing protease activities and for HPLC derivatization by fluorescence detection.
Purity:
>97% (NMR)
SMILES:
COC1=CC=C2C(CC(O)=O)=CC(=O)OC2=C1
Solubility Chemicals:
Soluble in DMF (50 mg/ml), acetone or DMSO.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) H. Mita, et al.; Anal. Biochem. 180, 131 (1989) | (2) C.G. Knight; Lett. Pept. Sci. 5, 1 (1998) | (3) C. Charitos, et al.; J. Pept. Res. 56, 373 (2000) | (4) G.A. Bannikov, et al.; J. Biol. Chem. 277, 16022 (2002) | (5) A. Ciencialova, et al.; J. Pept. Sci. 10, 470 (2004) | (6) L.E. Yandek, et al.; Biophys. J. 92, 2434 (2007) | (7) A. Lesner, et al.; Anal. Biochem. 375, 306 (2008)
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