Catalog No.:AA008MXN

783-08-4 | N-Benzylidene-4-methoxyaniline

Name: Name:N-Benzylidene-4-methoxyaniline
Brand: AABLOCKS
SKU: AA008MXN
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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA008MXN

Chemical Name:

N-Benzylidene-4-methoxyaniline

CAS Number:

783-08-4

Molecular Formula:

C25H28Cl3N7O2S

Molecular Weight:

596.9595

MDL Number:

MFCD00025797

SMILES:

CN1CCN(CC1)c1ccc2c(c1)nc([nH]2)c1ccc2c(c1)nc([nH]2)c1ccc(cc1)S(=O)(=O)N.Cl.Cl.Cl

NSC Number:

95582

Properties

Computed Properties

Complexity:

213

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

2.8

Downstream Synthesis Route

783-08-4

17377-95-6

[1]Organometallics,2019,vol.38,p.2610-2623

[2]OrganicLetters,2014,vol.16,p.2558-2561

[3]NewJournalofChemistry,2020,vol.44,p.11330-11335

[4]AsianJournalofChemistry,2011,vol.23,p.4101-4103

[5]Synlett,2014,vol.25,p.795-798

[6]Synthesis,1981,p.442-444

[7]AngewandteChemie-InternationalEdition,2010,vol.49,p.7548-7552

[8]Chemistry-AEuropeanJournal,2012,vol.18,p.13885-13892

[9]Patent:CN104892336,2017,B.Locationinpatent:Paragraph0056;0057;0058;0059;0060;0061;0062-0065

[10]JournaloftheAmericanChemicalSociety,2019,vol.141,p.11677-11685

[11]Chemicalandpharmaceuticalbulletin,1986,vol.34,p.4817-4820

[12]OrganicandBiomolecularChemistry,2013,vol.11,p.6934-6939

[13]Patent:WO2013/153408,2013,A1.Locationinpatent:Paragraph00137;00139

[14]Patent:US2015/73165,2015,A1.Locationinpatent:Paragraph0293;0295

[15]AppliedOrganometallicChemistry,2019,vol.33

[16]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1987,vol.26,p.199-200

[17]JournalofChemicalResearch,2015,vol.39,p.390-393

[18]Catalysisscienceandtechnology,2013,vol.3,p.3111-3116

[19]Catalysisscienceandtechnology,2015,vol.5,p.1452-1458

[20]ChemistryLetters,1996,p.407-408

[21]ChemSusChem,2012,vol.5,p.396-399

[22]Chemistry-AEuropeanJournal,2019,vol.25,p.238-245

[23]TetrahedronLetters,2012,vol.53,p.416-418

[24]OrganicandBiomolecularChemistry,2018,vol.16,p.9368-9372

[25]JournalofMolecularCatalysisA:Chemical,2014,vol.393,p.134-141

[26]RSCAdvances,2017,vol.7,p.31795-31799

[27]Tetrahedron,1997,vol.53,p.6907-6916

[28]SyntheticCommunications,2001,vol.31,p.1581-1586

[29]EuropeanJournalofInorganicChemistry,2018,vol.2018,p.3195-3202

[30]JournalofOrganicChemistry,2018,vol.83,p.11886-11895

[31]InorganicChemistry,2018,vol.57,p.14582-14593

[32]SyntheticCommunications,2009,vol.39,p.1332-1341

[33]NewJournalofChemistry,2019,vol.43,p.16524-16529

[34]NatureChemistry,2019,vol.11,p.669-675

[35]ChemSusChem,2019,vol.12,p.3089-3093

[36]DaltonTransactions,2012,vol.41,p.14557-14567

[37]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2001,vol.40,p.1134-1139

[38]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1921,vol.172,p.281 BulletindelaSocieteChimiquedeFrance,1921,vol.<4>29,p.107

[39]JournalofOrganicChemistry,1957,vol.22,p.1068

[40]Synlett,2000,p.1565-1568

[41]Tetrahedron,2005,vol.61,p.5725-5734

[42]TetrahedronLetters,1983,vol.24,p.5113-5116

[43]Chemicalandpharmaceuticalbulletin,1971,vol.19,p.1722-1727

[44]AdvancedSynthesisandCatalysis,2009,vol.351,p.1390-1394

[45]AngewandteChemie-InternationalEdition,2010,vol.49,p.2058-2062

[46]OrganicandBiomolecularChemistry,2011,vol.9,p.1927-1937

[47]ARKIVOC,2011,vol.2011,p.149-161

[48]GreenChemistry,2011,vol.13,p.2576-2584

[49]ChemicalCommunications,2012,vol.48,p.151-153

[50]TetrahedronLetters,2013,vol.54,p.6407-6410

[51]Chemistry-AnAsianJournal,2014,vol.9,p.328-337

[52]JournaloftheChineseChemicalSociety,2013,vol.60,p.1267-1271

[53]AngewandteChemie-InternationalEdition,2014,vol.53,p.10742-10746 Angew.Chem.,2014,vol.126,p.10918-10922,5

[54]TetrahedronLetters,2015,vol.56,p.3393-3395

[55]ChineseJournalofCatalysis,2015,vol.36,p.1191-1196

[56]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2015,vol.54B,p.1252-1259

[57]Organometallics,2016,vol.35,p.2930-2937

[58]DaltonTransactions,2016,vol.45,p.12835-12845

[59]AngewandteChemie-InternationalEdition,2017,vol.56,p.5556-5560 Angew.Chem.,2017,vol.129,p.5648-5652,5

[60]AdvancedSynthesisandCatalysis,2017,vol.359,p.2580-2584

[61]JournaloftheAmericanChemicalSociety,2017,vol.139,p.16584-16590

[62]JournalofOrganometallicChemistry,2017,vol.846,p.208-216

[63]AdvancedSynthesisandCatalysis,2018,vol.360,p.1054-1059

[64]ChemicalCommunications,2018,vol.54,p.4302-4305

[65]InorganicaChimicaActa,2019,vol.486,p.119-128

[66]Tetrahedron,2018,vol.74,p.7209-7217

[67]InorganicChemistry,2018,vol.57,p.15069-15078

[68]AdvancedSynthesisandCatalysis,2019,vol.361,p.2849-2854

[69]Molecularcatalysis,2019,vol.476

[70]AdvancedSynthesisandCatalysis,2019,vol.361,p.4781-4789

[71]AppliedOrganometallicChemistry,2020,vol.34

[72]EuropeanJournalofOrganicChemistry,2020,vol.2020,p.3508-3514

[73]OrganicandBiomolecularChemistry,2020,vol.18,p.3853-3857

588-53-4

74-88-4

783-08-4

[1]Sowa,Sylwia;Pietrusiewicz,K.Michał[EuropeanJournalofOrganicChemistry,2019,vol.2019,#5,p.923-938]

[2]Philipp[ChemischeBerichte,1892,vol.25,p.3248]

56146-83-9

783-08-4

126178-19-6

[1]TetrahedronLetters,1989,vol.30,p.2869-2872

783-08-4

139007-45-7

cis-1-(4-methoxyphenyl)-3-phenylmethyloxy-4-phenyl-2-azetidinone

trans-1-(4-methoxyphenyl)-3-phenylmethoxy-4-phenylazetidin-2-one

[1]Annunziata,Rita;Benaglia,Maurizio;Cinquini,Mauro;Cozzi,Franco;Raimondi,Laura[Tetrahedron,1994,vol.50,#19,p.5821-5828]

[2]Annunziata,Rita;Benaglia,Maurizio;Cinquini,Mauro;Cozzi,Franco;Raimondi,Laura[Tetrahedron,1994,vol.50,#19,p.5821-5828]

70591-20-7

783-08-4

139616-39-0

[1]SyntheticCommunications,1992,vol.22,p.63-71

Literature

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