Catalog No.:AA003LWM

92-53-5 | 4-Phenylmorpholine

Name: Name:4-Phenylmorpholine
Brand: AABLOCKS
SKU: AA003LWM
Availability: InStock
Rating: 90 (10 reviews)

Pack Size

Purity

Availability

Price(USD)

Quantity

98%

in stock

$6.00 $4.00

- +

10g

98%

in stock

$8.00 $6.00

- +

25g

98%

in stock

$18.00 $13.00

- +

100g

98%

in stock

$45.00 $32.00

- +

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003LWM

Chemical Name:

4-Phenylmorpholine

CAS Number:

92-53-5

Molecular Formula:

C10H13NO

Molecular Weight:

163.2163

MDL Number:

MFCD00006166

SMILES:

O1CCN(CC1)c1ccccc1

NSC Number:

2628

Properties

BP:

264.8 °C at 760 mmHg

Form:

Solid

MP:

51-54 °C(lit.)

Refractive Index:

1.5400 (estimate)

Solubility:

3.46 g/L

Storage:

Inert atmosphere;Room Temperature;

Computed Properties

Complexity:

126

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

1.4

Upstream Synthesis Route

110-91-8

108-94-1

670-80-4

92-53-5

[1]CatalysisScienceandTechnology,2016,vol.6,#11,p.3929-3937

[2]CatalysisScienceandTechnology,2016,vol.6,#11,p.3929-3937

110-91-8

108-94-1

6425-41-8

670-80-4

92-53-5

[1]CatalysisScienceandTechnology,2016,vol.6,#11,p.3929-3937

92-53-5

2524-67-6

[1]JournaloftheAmericanChemicalSociety,1939,vol.61,p.2552

92-53-5

30483-75-1

[1]OrganicLetters,2017,vol.19,#16,p.4243-4246

[2]JournalofChemicalResearch,2014,vol.38,#10,p.593-596

[3]OrganicLetters,2015,vol.17,#12,p.2886-2889

[4]Synthesis,2009,#21,p.3672-3676

[5]SyntheticCommunications,2010,vol.40,#19,p.2954-2962

[6]BulletinoftheKoreanChemicalSociety,2012,vol.33,#8,p.2619-2622

[7]Tetrahedron,2012,vol.68,#51,p.10476-10481,6

[8]TetrahedronLetters,2007,vol.48,#45,p.7969-7973

[9]EuropeanJournalofMedicinalChemistry,2018,vol.157,p.320-332

[10]Patent:EP1323716,2003,A1,

[11]Patent:US7008950,2006,B1,.Locationinpatent:Page/Pagecolumn37

[12]Patent:WO2003/104227,2003,A1,.Locationinpatent:Page52,53

[13]Patent:WO2004/16606,2004,A1,.Locationinpatent:Page23

[14]Patent:WO2004/13138,2004,A2,.Locationinpatent:Page23

[15]Patent:WO2004/13135,2004,A1,.Locationinpatent:Page47-48

[16]TetrahedronLetters,2006,vol.47,#23,p.3889-3892

[17]Patent:US4139704,1979,A,

[18]Patent:US4178447,1979,A,

92-53-5

30483-75-1

87698-82-6

[1]JournalofOrganicChemistry,2008,vol.73,#17,p.6849-6852

Downstream Synthesis Route

110-91-8

108-86-1

92-53-5

[1]EuropeanJournalofInorganicChemistry,2005,p.5011-5017

[2]Patent:US2014/213785,2014,A1.Locationinpatent:Paragraph0039-0043;0046

[3]JournalofOrganometallicChemistry,2009,vol.694,p.1473-1481

[4]Polyhedron,2011,vol.30,p.195-200

[5]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.3319-3322

[6]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.1908-1914

[7]Patent:JP2018/127451,2018,A.Locationinpatent:Paragraph0092;0093;0094;0096

[8]Patent:CN105801625,2016,A.Locationinpatent:Paragraph0050;0051;0052;0053;0054;0057;0058;0060-64

[9]JournalofOrganometallicChemistry,2018,vol.861,p.125-130

[10]Tetrahedron,2008,vol.64,p.9507-9514

[11]JournalofOrganometallicChemistry,2017,vol.851,p.210-217

[12]JournalofOrganicChemistry,2008,vol.73,p.3047-3062

[13]JournaloftheIranianChemicalSociety,2015,vol.12,p.2057-2064

[14]JournalofOrganicChemistry,2002,vol.67,p.6479-6486

[15]DaltonTransactions,2008,vol.8,p.938-945

[16]AppliedOrganometallicChemistry,2013,vol.27,p.704-706

[17]JournalofPhysicsandChemistryofSolids,2020,vol.138

[18]AppliedOrganometallicChemistry,2020

[19]JournalofOrganometallicChemistry,2019,vol.899

[20]OrganicLetters,2010,vol.12,p.1640-1643

[21]AdvancedSynthesisandCatalysis,2012,vol.354,p.1061-1068

[22]JournalofOrganicChemistry,2013,vol.78,p.7575-7581

[23]AdvancedSynthesisandCatalysis,2008,vol.350,p.2767-2777

[24]TetrahedronLetters,2014,vol.55,p.4098-4101

[25]ChemicalCommunications,2014,vol.50,p.9454-9457

[26]Patent:US2016/152583,2016,A1.Locationinpatent:Paragraph0112-0114

[27]Chemistry-AEuropeanJournal,2006,vol.12,p.3636-3646

[28]JournaloftheChineseChemicalSociety,2010,vol.57,p.604-611

[29]JournalofOrganometallicChemistry,2016,vol.803,p.142-149

[30]ChemicalCommunications,2010,vol.46,p.1103-1105

[31]NewJournalofChemistry,2016,vol.40,p.1287-1296

[32]InorganicaChimicaActa,2015,vol.427,p.226-231

[33]AppliedOrganometallicChemistry,2018,vol.32

[34]TetrahedronLetters,2013,vol.54,p.1120-1124

[35]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.6515-6525

[36]OrganicandBiomolecularChemistry,2020,vol.18,p.450-464

[37]Synlett,2005,p.1275-1278

[38]Synthesis,2018,vol.50,p.3911-3920

[39]OrganicLetters,2005,vol.7,p.1169-1172

[40]ChemistryLetters,2011,vol.40,p.934-935

[41]JournalofOrganometallicChemistry,2010,vol.695,p.1768-1775

[42]GreenChemistry,2018,vol.20,p.5346-5357

[43]Synlett,2008,p.2540-2546

[44]OrganicLetters,2008,vol.10,p.4513-4516

[45]Catalysisscienceandtechnology,2015,vol.5,p.2378-2383

[46]DaltonTransactions,2019,vol.48,p.7203-7210

[47]JournalofOrganicChemistry,1993,vol.58,p.3156-3157

[48]TetrahedronLetters,2012,vol.53,p.6657-6661

[49]JournalofOrganometallicChemistry,2015,vol.781,p.23-34

[50]JournalofOrganicChemistry,2005,vol.70,p.8107-8109

[51]TetrahedronLetters,2016,vol.57,p.1532-1536

[52]AppliedOrganometallicChemistry,2014,vol.28,p.809-813

[53]JournalofOrganicChemistry,2008,vol.73,p.8639-8642

[54]OrganicandBiomolecularChemistry,2019,vol.17,p.1722-1726

[55]OrganicLetters,2012,vol.14,p.3056-3059

[56]SyntheticCommunications,2010,vol.40,p.222-228

[57]NewJournalofChemistry,2019,vol.43,p.19274-19278

[58]Tetrahedron,2015,vol.71,p.7931-7937

[59]Synthesis,2002,p.1597-1600

[60]AngewandteChemie-InternationalEdition,2009,vol.48,p.7398-7401 AngewandteChemie,2009,vol.121,p.7534-7537

[61]TetrahedronLetters,2010,vol.51,p.3910-3912

[62]JournaloftheAmericanChemicalSociety,2017,vol.139,p.9144-9147

[63]Synlett,2006,p.3105-3109

[64]Synthesis,2014,vol.46,p.3356-3364

[65]InorganicaChimicaActa,2015,vol.425,p.67-75

[66]JournalofOrganicChemistry,2004,vol.69,p.6504-6506

[67]Tetrahedron,2013,vol.69,p.1038-1042

[68]JournaloftheAmericanChemicalSociety,2018,vol.140,p.7667-7673

[69]JournalofOrganicChemistry,2020,vol.85,p.3234-3244

[70]JournalofOrganicChemistry,2011,vol.76,p.1180-1183

[71]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,p.1894-1908

[72]Science,2019,vol.365,p.360-366

[73]GreenChemistry,2010,vol.12,p.276-281

[74]JournalofCatalysis,2016,vol.341,p.205-220

[75]JournalofOrganicChemistry,1957,vol.22,p.832

[76]Synlett,2004,p.1747-1750

[77]Chemistry-AEuropeanJournal,2008,vol.14,p.2443-2452

[78]Tetrahedron,2009,vol.65,p.1180-1187

[79]JournalofOrganometallicChemistry,2009,vol.694,p.113-121

[80]InorganicaChimicaActa,2010,vol.363,p.1262-1268

[81]EuropeanJournalofInorganicChemistry,2011,p.1937-1952

[82]JournalofCatalysis,2009,vol.268,p.318-328

[83]OrganicLetters,2012,vol.14,p.4182-4185

[84]JournalofOrganometallicChemistry,2012,vol.720,p.7-18,12

[85]JournalofChemicalResearch,2013,vol.37,p.99-101

[86]JournalofOrganometallicChemistry,2013,vol.736,p.1-8

[87]RSCAdvances,2013,vol.3,p.10707-10721

[88]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.2070-2076

[89]JournalofInclusionPhenomenaandMacrocyclicChemistry,2015,vol.82,p.79-91

[90]JournalofOrganicChemistry,2015,vol.80,p.6794-6813

[91]Chemistry-AnAsianJournal,2016,vol.11,p.351-355

[92]Chemistry-AEuropeanJournal,2017,vol.23,p.6663-6674

[93]AngewandteChemie-InternationalEdition,2016,vol.55,p.12868-12872 Angew.Chem.,2016,vol.128,p.13060-13064,5

[94]OrganicLetters,2018,vol.20,p.1995-1998

[95]DaltonTransactions,2018,vol.47,p.10264-10272

[96]Patent:CN109574942,2019,A.Locationinpatent:Paragraph0052;0053

[97]CatalysisLetters,2020,vol.150,p.1669-1678

92-53-5

14368-49-1

100848-21-3

[1]BulletinofUniversityofOsakaPrefecture,SeriesA:EngineeringandNaturalSciences,1956,vol.<A>4,p.123,130

92-53-5

670-54-2

109504-23-6

[1]JournaloftheAmericanChemicalSociety,1958,vol.80,p.2806,2808

92-53-5

100-39-0

4-benzyl-4-phenyl-morpholinium;bromide

[1]Patent:US2437833,1946,

Literature

Title: Antitubercular nitrofuran isoxazolines with improved pharmacokinetic properties.

Journal: Bioorganic & medicinal chemistry 20121015

Title: Synthesis of some chalcones and pyrazolines carrying morpholinophenyl moiety as potential anti-inflammatory agents.

Journal: Archiv der Pharmazie 20110401

Title: Oxidation of fluoroquinolone antibiotics and structurally related amines by chlorine dioxide: Reaction kinetics, product and pathway evaluation.

Journal: Water research 20101201

Title: tert-Butyl 6-amino-3,4-dihydro-2H-1,4-benzoxazine-4-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20101201

Title: tert-Butyl 6-acetamido-3,4-dihydro-2H-1,4-benzoxazine-4-carboxyl-ate.

Journal: Acta crystallographica. Section E, Structure reports online 20101001

Title: Synthesis and pharmacological evaluation of schiff bases of 4-(2-aminophenyl)-morpholines.

Journal: Indian journal of pharmaceutical sciences 20090101

Title: A xerogel-sequestered selenoxide catalyst for brominations with hydrogen peroxide and sodium bromide in an aqueous environment.

Journal: The Journal of organic chemistry 20080905

Title: Further studies on hepatitis C virus NS5B RNA-dependent RNA polymerase inhibitors toward improved replicon cell activities: benzimidazole and structurally related compounds bearing the 2-morpholinophenyl moiety.

Journal: Bioorganic & medicinal chemistry letters 20070601

Title: Adsorption and oxidation of fluoroquinolone antibacterial agents and structurally related amines with goethite.

Journal: Chemosphere 20070101

Title: Oxidative transformation of fluoroquinolone antibacterial agents and structurally related amines by manganese oxide.

Journal: Environmental science & technology 20050615

Quotation Request

Company Name:

Contact Person:

Email:

Quantity Required:

Country: