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ChemicalBook--->CAS DataBase List--->92944-71-3

92944-71-3

92944-71-3 Structure

92944-71-3 Structure
IdentificationBack Directory
[Name]

BENZOPHENONE-4-MALEIMIDE
[CAS]

92944-71-3
[Synonyms]

AKOS MSC-0079
1-(4-Benzoylphenyl)-
BENZOPHENONE-4-MALEIMIDE
4-(MALEIMIDO)BENZOPHENONE
4-(N-MALEIMIDO)BENZOPHENONE
4-(Maleinimido)benzophenone
1-(4-BENZOYLPHENYL)-1H-PYRROLE-2,5-DIONE
Benzophenone-4-MaleiMide [4-(N-MaleiMido)benzophenone]
[Molecular Formula]

C17H11NO3
[MDL Number]

MFCD00079465
[MOL File]

92944-71-3.mol
[Molecular Weight]

277.27
Chemical PropertiesBack Directory
[Appearance]

Light Beige Solid
[Melting point ]

155-157°C
[Boiling point ]

472.9±28.0 °C(Predicted)
[density ]

1.330±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

chloroform: 50 mg/mL
[form ]

Solid
[pka]

-3.80±0.20(Predicted)
[color ]

Light Beige
Hazard InformationBack Directory
[Chemical Properties]

Light Beige Solid
[Uses]

A heterobifunctional cross-linking reagent containing a sulfhydryl-specific group and a photo-active group. Typically, coupled initially by thioether to molecule containing free sulfhydryl buffered at pH 6.8 (6.5-7.0). Second bonding occurs during UV irradiation (250 nm) via diradical excited state. Benzophenones demonstrate greater specificity for C-H insertion and are more stable in water than analogous reagents. In general they are more efficient in attachment because they may be repeatedly irradiated; however, a more intense irradiation may be required. The benzophenone is not sensitive to
[Uses]

A sulfhydryl reactive heterobifunctional photocrosslinking reagent. It generates photoactivatable conjugates from thiols
[Uses]

Maleimide-containing benzophenone as photoinitiator
[reaction suitability]

reagent type: cross-linking reagent
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

29251900
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