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4-Bromomethyl-7-methoxycoumarin

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4-Bromomethyl-7-methoxycoumarin Basic information

Product Name:
4-Bromomethyl-7-methoxycoumarin
Synonyms:
  • Br-Mmc (=4-Bromomethyl-7-methoxycoumarin) [for HPLC Labeling]
  • BR-MMC (=4-BROMOETHYL-7-METHOXYCOUMARIN)
  • 4-BROMOMETHYL-7-METHOXYCOUMARIN [FOR HPLC LABELING]
  • BMC, Br-Mmc
  • 2H-1-Benzopyran-2-one, 4-(bromomethyl)-7-methoxy-
  • 4-(Bromomethyl)-7-methoxychromen-2-one
  • 4-(Bromomethyl)-7-methoxy-2H-1-benzopyran-2-one
  • 7-Methoxy-4-bromomethylcoumarin
CAS:
35231-44-8
MF:
C11H9BrO3
MW:
269.09
EINECS:
252-448-3
Product Categories:
  • Carboxyl Group Labeling Reagents for Fluorescence HPLC
  • Fluorescence Detection (HPLC Labeling Reagents)
  • Coumarins
  • Fluorescent Labels and Indicators
  • HPLC Labeling Reagents
  • Fluorescent Labels & Indicators
  • Analytical Chemistry
Mol File:
35231-44-8.mol
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4-Bromomethyl-7-methoxycoumarin Chemical Properties

Melting point:
213-215 °C (lit.)
Boiling point:
385.3±42.0 °C(Predicted)
Density 
1.552±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
chloroform: soluble20mg/mL, clear, colorless to faintly yellow
form 
Powder and/or Chunks
color 
Off-white to light yellow or beige
Water Solubility 
insoluble
λmax
330 nm (MeOH)
BRN 
187211
Stability:
Stable, but moisture and light-sensitive. Combustible. Incompatible with strong oxidizing agents.
Major Application
Detection of nitrated explosives; measuring ultraviolet ray power; photoacid generators; polyurethane foams; photoresists silica nanoparticles
Biological Applications
Analyzing/detecting carboxylic acids;analyzing/labeling fatty acids; detecting nitric oxide; detecting/separating bile acids; labeling pyrimidine nucleobases; anticancer agents; biomedical trace analysis; herbicides; as a substrate for measuring histone acetyltransferases (HATs) activity, peptidases activity, sirtuin activity
LogP
2.730 (est)
CAS DataBase Reference
35231-44-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36-37/39
RIDADR 
1759
WGK Germany 
3
HazardClass 
8
PackingGroup 
III
HS Code 
29322090

MSDS

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4-Bromomethyl-7-methoxycoumarin Usage And Synthesis

Chemical Properties

Light Green-Yellow Crystals

Uses

4-Bromomethyl-7-methoxycoumarin has been used:

  • as derivatization reagent in determination of 5-fluorouracil (5-FU) in human plasma by HPLC-tandem mass spectrometry
  • as derivatization reagent in fluorescence detection of sodium monofluoroacetate (MFA-Na) in biological samples by HPLC
  • in the synthesis of new caged derivatives of hydrolysis-resistant 8-bromoadenosine cyclic 3′,5′-monophosphate (8-Br-cAMP) and 8-bromoguanosine cyclic 3′,5′-monophosphate (8-Br-cGMP)
  • in TLC and HPLC separation and fluorometric analysis of a wide range of naturally occurring acids, including bile and thromboxane B2

Uses

4-Bromomethyl-7-methoxycoumarin can be used as fluorescent label for fatty acids. For derivatization, TLC and HPLC separation, and fluorometric analysis of a wide range of naturally occurring acids, including bile and thromboxane B2.

Purification Methods

The coumarin crystallises from boiling AcOH; the crystals are washed with AcOH, EtOH and dried in a vacuum; 1HNMR (TFA) 3.97s, 4.57s, 6.62s, 6.92-7.19m and 7.80d. [Secrist et al. Biochem Biophys Res Commun 45 1262 1971, Dünges Anal Chem 49 442 1977, Beilstein 18 III/IV 348.]

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