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7465-88-5,MFCD00025810
Catalog No.:AA00FFTV

7465-88-5 | N-Phenyl-4-methoxybenzamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95+%
in stock  
$34.00   $24.00
- +
250mg
95+%
in stock  
$56.00   $39.00
- +
1g
95+%
in stock  
$150.00   $105.00
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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:
AA00FFTV
Chemical Name:
N-Phenyl-4-methoxybenzamide
CAS Number:
7465-88-5
Molecular Formula:
C14H13NO2
Molecular Weight:
227.2585
MDL Number:
MFCD00025810
SMILES:
COc1ccc(cc1)C(=O)Nc1ccccc1
NSC Number:
404049
Properties
Computed Properties
 
Complexity:
241  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.6  

Downstream Synthesis Route

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[2]JournaloftheAmericanChemicalSociety,1920,vol.42,p.607

[1]AngewandteChemie-InternationalEdition,2015,vol.54,p.1312-1315    Angew.Chem.,2015,vol.54,p.1328-1331,4

[2]EuropeanJournalofOrganicChemistry,2010,p.326-332

[3]RSCAdvances,2015,vol.5,p.90521-90524

[4]Synlett,2021,vol.32,p.718-722

[5]Organometallics,2013,vol.32,p.4677-4683

[6]Tetrahedron,2011,vol.67,p.8532-8535

[7]JournalofChemicalResearch,2015,vol.39,p.654-656

[8]NewJournalofChemistry,2017,vol.41,p.2328-2332

[9]Patent:CN104086345,2016,B.Locationinpatent:Paragraph0046-0048

[10]ZhurnalObshcheiKhimii,1958,vol.28,p.739,740;engl.Ausg.S.719

[11]JournalofOrganicChemistry,2015,vol.80,p.11993-11998

[12]ScienceChinaChemistry,2016,vol.59,p.478-481

[13]RSCAdvances,2022,vol.12,p.7621-7625

[1]JournaloftheIndianChemicalSociety,2004,vol.81,p.885-887

[2]ChemischeBerichte,1964,vol.97,p.472-479

[3]ChemischesZentralblatt,1929,vol.100,p.2156

[1]JournalofMedicinalChemistry,2004,vol.47,p.663-672

[2]TetrahedronLetters,2010,vol.51,p.6049-6051

[3]AdvancedSynthesisandCatalysis,2022,vol.364,p.1150-1155

[4]Molecules,2022,vol.27

[5]TetrahedronLetters,2004,vol.45,p.2285-2287

[6]OrganicLetters,2011,vol.13,p.2818-2821

[7]ChemicalCommunications,2013,vol.49,p.7412-7414

[8]Patent:WO2005/30729,2005,A1.Locationinpatent:Page/Pagecolumn37;42

[9]JournalofOrganicChemistryUSSR(EnglishTranslation),1984,vol.20,p.121-123    ZhurnalOrganicheskoiKhimii,1984,vol.20,p.134-137

[10]AnnalesdeChimie(Cachan,France),1848,vol.<3>23,p.345    JustusLiebigsAnnalenderChemie,1849,vol.70,p.44

[11]JournaloftheChemicalSociety.PerkintransactionsI,1987,p.1153-1158

[12]MedicinalChemistryResearch,1997,vol.7,p.180-191

[13]OrganicLetters,2003,vol.5,p.849-852

[14]JournaloftheChemicalSociety.PerkinTransactions2(2001),2002,vol.2,p.312-317

[15]TetrahedronLetters,2008,vol.49,p.1636-1640

[16]SyntheticCommunications,2011,vol.41,p.2888-2898

[17]JournalofMedicinalChemistry,2012,vol.55,p.1645-1661

[18]Chemistry-AEuropeanJournal,2013,vol.19,p.11039-11050

[19]EuropeanJournalofMedicinalChemistry,2013,vol.67,p.166-174

[20]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.2051-2060

[21]JournalofOrganicChemistry,2016,vol.81,p.309-317

[22]OrganicLetters,2017,vol.19,p.3799-3802

[23]OrganicLetters,2019,vol.21,p.237-241

[24]ChemicalCommunications,2020,vol.56,p.1565-1568

[25]JournalofOrganicChemistry,2020,vol.85,p.7433-7445

[26]OrganicLetters,2021,vol.23,p.4843-4848

[1]JournaloftheChemicalSociety.PerkintransactionsI,1987,p.1153-1158

[2]JournalofMedicinalChemistry,2004,vol.47,p.663-672

[3]AmericanChemicalJournal,1903,vol.30,p.37

[4]ChemischeBerichte,1962,vol.95,p.126-136

[5]Heterocycles,1996,vol.43,p.1201-1209

[6]JournaloftheChemicalSociety.PerkinTransactions2(2001),2002,vol.2,p.312-317

[7]JournalofMedicinalChemistry,2012,vol.55,p.1645-1661

[8]OrganicLetters,2014,vol.16,p.2822-2825

[9]MendeleevCommunications,2015,vol.25,p.126-128

[10]JournalofOrganicChemistry,2016,vol.81,p.309-317

[11]TetrahedronLetters,2018,vol.59,p.2368-2371

[12]OrganicandBiomolecularChemistry,2018,vol.16,p.7657-7662

[13]JournalofOrganicChemistry,2020,vol.85,p.7433-7445

[14]Molecules,2022,vol.27

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

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