Cas no 92944-71-3 (4-(Maleimido)benzophenone)

4-(Maleimido)benzophenone structure
4-(Maleimido)benzophenone structure
Product Name:4-(Maleimido)benzophenone
CAS No:92944-71-3
MF:C17H11NO3
MW:277.274144411087
MDL:MFCD00079465
CID:807060
PubChem ID:57654429
Update Time:2024-10-26

4-(Maleimido)benzophenone Chemical and Physical Properties

Names and Identifiers

    • 1H-Pyrrole-2,5-dione,1-(4-benzoylphenyl)-
    • 4-(Maleimido)benzophenone
    • 1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione
    • 1-(4-benzoylphenyl)pyrrole-2,5-dione
    • 4-(Maleimido)benzoph
    • Benzophenone-4-maleimide [4-(N-Maleimido)benzophenone]
    • 1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione (ACI)
    • N-(4-Benzoylphenyl)maleimide
    • N-(p-Phenylcarbonylphenyl)maleimide
    • M3259
    • Benzophenone-4-maleimide
    • OZIZEXQRIOURIJ-UHFFFAOYSA-N
    • DTXSID50239207
    • 4-Maleimidobenzophenone
    • AKOS004115282
    • 92944-71-3
    • 1H-Pyrrole-2,5-dione, 1-(4-benzoylphenyl)-
    • DTXCID30161698
    • 1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione; N-(4-Benzoylphenyl)maleimide;
    • MFCD00079465
    • CS-0117778
    • SCHEMBL339889
    • BS-49340
    • DB-057349
    • E79368
    • 4-(N-Maleimido)benzophenone
    • MDL: MFCD00079465
    • Inchi: 1S/C17H11NO3/c19-15-10-11-16(20)18(15)14-8-6-13(7-9-14)17(21)12-4-2-1-3-5-12/h1-11H
    • InChI Key: OZIZEXQRIOURIJ-UHFFFAOYSA-N
    • SMILES: O=C1N(C2C=CC(C(C3C=CC=CC=3)=O)=CC=2)C(=O)C=C1

Computed Properties

  • Exact Mass: 277.07400
  • Monoisotopic Mass: 277.074
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 3
  • Complexity: 450
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 54.4A^2

Experimental Properties

  • Density: 1.33
  • Melting Point: 155-157°C
  • Boiling Point: 472.9°Cat760mmHg
  • Flash Point: 223.7°C
  • Refractive Index: 1.651
  • Solubility: chloroform: 50?mg/mL
  • PSA: 54.45000
  • LogP: 2.41200

4-(Maleimido)benzophenone Security Information

  • Symbol: GHS07
  • Signal Word:Warning
  • Hazard Statement: H315-H319-H335
  • Warning Statement: P261-P305+P351+P338
  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3
  • Hazard Category Code: 36/37/38
  • Safety Instruction: S26; S36
  • Hazardous Material Identification: Xi
  • Risk Phrases:R36/37/38
  • Storage Condition:2-8°C

4-(Maleimido)benzophenone Customs Data

  • HS CODE:2925190090
  • Customs Data:

    China Customs Code:

    2925190090

    Overview:

    2925190090 Other imides and their derivative salts. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

4-(Maleimido)benzophenone Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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M3259-50MG
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TRC
M133000-25mg
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25mg
$ 121.00 2023-09-07
TRC
M133000-50mg
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50mg
$ 138.00 2023-09-07
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M133000-100mg
4-(Maleimido)benzophenone
92944-71-3
100mg
$ 167.00 2023-09-07
TRC
M133000-250mg
4-(Maleimido)benzophenone
92944-71-3
250mg
$391.00 2023-05-18
TRC
M133000-500mg
4-(Maleimido)benzophenone
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4-(Maleimido)benzophenone Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Acetic anhydride ,  Sodium acetate
Reference
Rational Design of Calpain Inhibitors Based on Calpastatin Peptidomimetics
Low, Kristin E.; Ler, Spencer; Chen, Kevin J.; Campbell, Robert L.; Hickey, Jennifer L.; et al, Journal of Medicinal Chemistry, 2016, 59(11), 5403-5415

Production Method 2

Reaction Conditions
1.1 Solvents: Toluene ;  3 h, reflux
1.2 Reagents: Sodium acetate Solvents: Acetic anhydride ;  2 h, reflux
1.3 Reagents: Sodium bicarbonate ;  neutralized
Reference
Synthesis and characterization of styrene/maleimide copolymers with high poling stability of dipolar chromophore
Arora, S.; Kumar, S., Optoelectronics and Advanced Materials, 2009, 3(12), 1359-1364

Production Method 3

Reaction Conditions
1.1 Solvents: Diethyl ether ;  1 h, reflux
1.2 Reagents: Sodium acetate Solvents: Acetic anhydride ;  0.5 h, 90 °C
1.3 Reagents: Water ;  cooled
Reference
Design, synthesis and biochemical evaluation of novel ethanoanthracenes and related compounds to target Burkitt's lymphoma
Byrne, Andrew J.; Bright, Sandra A.; McKeown, James P.; O'Brien, John E.; Twamley, Brendan; et al, Pharmaceuticals, 2020, 13(1),

Production Method 4

Reaction Conditions
Reference
Synthesis of new bifunctional maleimide compounds for the preparation of chemoimmunoconjugates
Beyer, U.; Kruger, M.; Schumacher, P.; Unger, C.; Kratz, F., Monatshefte fuer Chemie, 1997, 128(1), 91-102

Production Method 5

Reaction Conditions
Reference
Maleimide derivatives
, Japan, , ,

Production Method 6

Reaction Conditions
1.1 Solvents: Diethyl ether ;  rt; rt → reflux; 8 h, reflux
1.2 Reagents: Acetic anhydride ,  Sodium acetate ;  5 h, 80 °C
Reference
Through-Space Charge-Transfer Thermally Activated Delayed Fluorescence Alternating Donor-Acceptor Copolymers for Nondoped Solution-Processable OLEDs
Belousov, George K.; Vaitusionak, Aliaksei A.; Vasilenko, Irina V.; Ghasemi, Melika ; Andruleviciene, Viktorija; et al, Macromolecules (Washington, 2023, 56(7), 2686-2699

Production Method 7

Reaction Conditions
Reference
Reaction of acyl chlorides with N-phenylimides of maleic and itaconic acids
Sanzhizhapov, D. B.; Mognonov, D. M.; Khakhinov, V. V.; Radnaeva, L. D.; Erdyneev, N. S., Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, 1984, (4), 118-20

Production Method 8

Reaction Conditions
1.1 Reagents: Acetic anhydride ,  Sodium acetate ;  30 min, 95 °C; 95 °C → rt
1.2 Solvents: Water ;  30 min, cooled
Reference
Effect of Polymerizable Photoinitiators on the UV-polymerization behaviors of photosensitive polysiloxane
Jiang, Bo; Zhang, Tong; Zhao, Liwei; Xu, Zhiming; Huang, Yudong, Journal of Polymer Science, 2017, 55(10), 1696-1705

Production Method 9

Reaction Conditions
Reference
Antineoplastic cytotoxic agent conjugates with transferrin, albumin and polyethylene glycol
, World Intellectual Property Organization, , ,

Production Method 10

Reaction Conditions
Reference
Antineoplastic transferrin and albumin conjugates of cytostatic compounds selected from anthracyclines, alkylating agents, antimetabolites, and cisplatin analogs
, Germany, , ,

4-(Maleimido)benzophenone Raw materials

4-(Maleimido)benzophenone Preparation Products

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