ChemicalBook >> CAS DataBase List >>4-(N-Maleimido)benzophenone

4-(N-Maleimido)benzophenone

CAS No.
92944-71-3
Chemical Name:
4-(N-Maleimido)benzophenone
Synonyms
AKOS MSC-0079;1-(4-Benzoylphenyl)-;BENZOPHENONE-4-MALEIMIDE;4-(MALEIMIDO)BENZOPHENONE;4-(N-MALEIMIDO)BENZOPHENONE;4-(Maleinimido)benzophenone;N-(4-benzoylphenyl)maleimide;1-(4-benzoylphenyl)pyrrole-2,5-dione;1-(4-BENZOYLPHENYL)-1H-PYRROLE-2,5-DIONE;1H-Pyrrole-2,5-dione, 1-(4-benzoylphenyl)-
CBNumber:
CB6293028
Molecular Formula:
C17H11NO3
Molecular Weight:
277.27
MDL Number:
MFCD00079465
MOL File:
92944-71-3.mol
MSDS File:
SDS
Last updated:2023-07-14 08:28:44

4-(N-Maleimido)benzophenone Properties

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

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29251900

4-(N-Maleimido)benzophenone price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich M9775 4-(N-Maleimido)benzophenone 92944-71-3 100mg $160 2022-05-15 Buy
TCI Chemical M3259 4-(N-Maleimido)benzophenone 92944-71-3 50MG $132 2024-03-01 Buy
TCI Chemical M3259 4-(N-Maleimido)benzophenone 92944-71-3 250MG $397 2024-03-01 Buy
TRC M133000 4-(Maleimido)benzophenone 92944-71-3 250mg $320 2021-12-16 Buy
TRC M133000 4-(Maleimido)benzophenone 92944-71-3 500mg $620 2021-12-16 Buy
Product number Packaging Price Buy
M9775 100mg $160 Buy
M3259 50MG $132 Buy
M3259 250MG $397 Buy
M133000 250mg $320 Buy
M133000 500mg $620 Buy

4-(N-Maleimido)benzophenone Chemical Properties,Uses,Production

Chemical Properties

Light Beige Solid

Uses

4-(N-Maleimido)benzophenone can be used as a sulfhydryl reactive heterobifunctional photocrosslinking reagent. It generates photoactivatable conjugates from thiols

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

Maleimide-containing benzophenone as photoinitiator

108-31-6
1137-41-3
92944-71-3
Synthesis of 4-(N-Maleimido)benzophenone from Maleic anhydride and 4-Aminobenzophenone

4-(N-Maleimido)benzophenone Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 62)Suppliers
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BENZOPHENONE-4-MALEIMIDE 4-(Maleinimido)benzophenone 1-(4-BENZOYLPHENYL)-1H-PYRROLE-2,5-DIONE 1-(4-Benzoylphenyl)- Benzophenone-4-MaleiMide [4-(N-MaleiMido)benzophenone] 4-(N-MALEIMIDO)BENZOPHENONE 4-(MALEIMIDO)BENZOPHENONE AKOS MSC-0079 1-(4-benzoylphenyl)pyrrole-2,5-dione N-(4-benzoylphenyl)maleimide 1H-Pyrrole-2,5-dione, 1-(4-benzoylphenyl)- 92944-71-3 Heterobifunctional Cross-Linking Reagents Crosslinking Proteomics Proteomics and Protein Expression Protein Modification BioChemical Maleimide Derivatives Cross Linking Reagents MTS & Sulfhydryl Active Reagents Linking Reagents Aromatics Heterocycles Heterobifunctional Cross-Linking Reagents Protein Modification Protein Structural Analysis Building Blocks Carbonyl Compounds Chemical Synthesis Crosslinking Cyclic Imides Organic Building Blocks Proteomics