ChemicalBook--->CAS DataBase List--->25392-41-0

25392-41-0

25392-41-0 Structure

25392-41-0 Structure
IdentificationBack Directory
[Name]

4-(CHLOROMETHYL)-7-HYDROXY-2H-CHROMEN-2-ONE
[CAS]

25392-41-0
[Synonyms]

BlueCMHC
EOS-61059
AKOS BBS-000001
AKOS BBS-00000158
OTAVA-BB BB7014350028
CELLTRACKER(TM) BLUE CMHC
ViVidFluor Cell Blue CMHC
4-(CHLOROMETHYL)-7-HYDROXYCOUMARIN
4-CHLOROMETHYL-7-HYDROXY-CHROMEN-2-ONE
4-(chloromethyl)-7-hydroxy-2-chromenone
4-(CHLOROMETHYL)-7-HYDROXY-2H-CHROMEN-2-ONE
4-(CHLOROMETHYL)-7-HYDROXY-2H-CHROMEN-2-ONE-2
2H-1-Benzopyran-2-one, 4-(chloroMethyl)-7-hydroxy-
CellHunt Blue CMHC [4-ChloroMethyl-7-hydroxycouMarin]
CellHunt Blue CMHC [4-Chloromethyl-7-hydroxycoumarin] [CellTracker Blue CMHC, TM of Molecular Probes]
[Molecular Formula]

C10H7ClO3
[MDL Number]

MFCD00467168
[MOL File]

25392-41-0.mol
[Molecular Weight]

210.61
Chemical PropertiesBack Directory
[Melting point ]

180-183°C
[Boiling point ]

409.6±45.0 °C(Predicted)
[density ]

1.442±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Solid
[pka]

7.72±0.20(Predicted)
[color ]

Off-white to pink
[Appearance]

Solid Powder
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2932209090
Hazard InformationBack Directory
[Description]

4-(Chloromethyl)-7-hydroxy-2H-chromen-2-one is a thiol-reactive, cell-permeant fluorescent probe that easily passes through cell membranes.

[Uses]

Fluorescent Thiol-Reactive cell permeant probe
[Synthesis]

Ethyl 4-chloroacetoacetate

638-07-3

Resorcinol

108-46-3

4-(CHLOROMETHYL)-7-HYDROXY-2H-CHROMEN-2-ONE

25392-41-0

A mixture of resorcinol (1.0 mmol), ethyl 4-chloroacetoacetate (1.5 mmol) and MNESA (0.075 g) was placed in a round-bottomed flask and the reaction was stirred at 90 °C. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was cooled to room temperature. The catalyst MNESA was separated from the reaction mixture using an external magnetic field. Subsequently, water was added to the reaction mixture and the target product, 4-chloromethyl-7-hydroxychromen-2-one, was extracted with ethyl acetate (EtOAc, 3 × 10 mL). The organic layers were combined, dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to give the crude product. For further purification, the crude product was recrystallized in ethanol to obtain high purity 4-chloromethyl-7-hydroxychromen-2-one.

[References]

[1] Tetrahedron Letters, 2005, vol. 46, # 36, p. 6119 - 6121
[2] Journal of Organic Chemistry, 2008, vol. 73, # 1, p. 287 - 290
[3] Synthetic Communications, 2008, vol. 38, # 13, p. 2082 - 2088
[4] Journal of Chemical Research, 2008, # 4, p. 232 - 234
[5] Synthetic Communications, 2010, vol. 40, # 22, p. 3358 - 3364
[Excitation / Emission Maximum]

348 nm/423 nm
Spectrum DetailBack Directory
[Spectrum Detail]

4-(CHLOROMETHYL)-7-HYDROXY-2H-CHROMEN-2-ONE(25392-41-0)1HNMR
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