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Home Bromides 13380-67-1
13380-67-1,MFCD00030664
Catalog No.:AA003S95

13380-67-1 | N-(4-Bromophenyl)maleimide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$16.00   $11.00
- +
5g
98%
in stock  
$71.00   $50.00
- +
25g
95%
in stock  
$230.00   $161.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003S95
Chemical Name:
N-(4-Bromophenyl)maleimide
CAS Number:
13380-67-1
Molecular Formula:
C10H6BrNO2
Molecular Weight:
252.0641
MDL Number:
MFCD00030664
SMILES:
O=C1C=CC(=O)N1c1ccc(cc1)Br
Properties
Properties
 
BP:
368.2±25.0 °C(Predicted)  
Form:
Solid  
MP:
135-137 °C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
275  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
1.8  

Downstream Synthesis Route

[1]JournalofOrganicChemistryUSSR(EnglishTranslation),1991,vol.27,p.1437-1443    ZhurnalOrganicheskoiKhimii,1991,vol.27,p.1641-1648

[2]JournalofOrganicChemistryUSSR(EnglishTranslation),1991,vol.27,p.1437-1443    ZhurnalOrganicheskoiKhimii,1991,vol.27,p.1641-1648

[3]JournalofOrganicChemistryUSSR(EnglishTranslation),1992,vol.28,p.1806-1813    ZhurnalOrganicheskoiKhimii,1992,vol.28,p.2244-2252

[1]JournaloftheAmericanChemicalSociety,1991,vol.113,p.5874-5876

13380-67-1   
2,5-diphenyl-3-trimethylsilylmethyl-1,3,4-thiadiazoliumtrifluoromethanesulfonate 
 
2,7a-diphenyl-5,6,7,7a-tetrahydropyrrolo2,1-b1,3,4thiadiazole-endo-6,7-N-(p-bromophenyl)dicarboxyimide 

[1]ChemicalCommunications,2001,p.1950-1951

[1]Synthesis,2003,p.1549-1552

[2]JournalofMedicinalChemistry,2009,vol.52,p.7410-7420

[3]OrganicLetters,2010,vol.12,p.1396-1399

[4]MagneticResonanceinChemistry,2009,vol.47,p.711-715

[5]BioorganicandMedicinalChemistry,2011,vol.19,p.2823-2834

[6]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,p.1166-1171

[7]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,p.1166-1171

[8]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,p.1166-1171

[9]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,p.1166-1171

[10]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2013,vol.52,p.1166-1171

[11]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2014,vol.53,p.392-398

[12]TetrahedronLetters,2015,vol.56,p.7150-7153

[13]JournalofHeterocyclicChemistry,2017,vol.54,p.1348-1354

[14]AsianJournalofChemistry,2017,vol.29,p.2285-2288

[1]Synlett,2017,vol.28,p.1336-1340

[2]Synlett,2010,p.2895-2898

[3]SyntheticCommunications,2004,vol.34,p.3073-3081

[4]BioorganicandMedicinalChemistry,2006,vol.14,p.5397-5401

Literature

Title: Chemical reactivity and antimicrobial activity of N-substituted maleimides.

Journal: Journal of enzyme inhibition and medicinal chemistry 20120201

Title: Antifungal, cytotoxic and SAR studies of a series of N-alkyl, N-aryl and N-alkylphenyl-1,4-pyrrolediones and related compounds.

Journal: Bioorganic & medicinal chemistry 20110501

Title: Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors.

Journal: Journal of medicinal chemistry 20091210

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SDS
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