Home Other Building Blocks 2524-67-6
2524-67-6,MFCD00006169
Catalog No.:AA00341H

2524-67-6 | 4-Morpholinoaniline

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1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$7.00   $5.00
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10g
97%
in stock  
$10.00   $7.00
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25g
97%
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$18.00   $12.00
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  • 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:
AA00341H
Chemical Name:
4-Morpholinoaniline
CAS Number:
2524-67-6
Molecular Formula:
C10H14N2O
Molecular Weight:
178.2310
MDL Number:
MFCD00006169
SMILES:
Nc1ccc(cc1)N1CCOCC1
NSC Number:
26334
Properties
Properties
 
BP:
368°C at 760 mmHg  
Form:
Solid  
MP:
132-135 °C(lit.)  
Refractive Index:
1.5250 (estimate)  
Solubility:
Soluble in chloroform, ethyl acetate.  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
149  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.7  

Upstream Synthesis Route

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[2]Chemistry-AnAsianJournal,2017,vol.12,#7,p.785-791

[3]Patent:EP2949647,2015,A1,.Locationinpatent:Paragraph0120

[4]EuropeanJournalofMedicinalChemistry,2016,vol.124,p.896-905

[5]Patent:US2013/45977,2013,A1,.Locationinpatent:Paragraph0215;0216;0217;0218

[6]RSCAdvances,2015,vol.5,#113,p.93433-93437

[7]Patent:CN104583195,2018,B,.Locationinpatent:Paragraph0486;0487;0491;0492;0493

[8]Patent:US2015/336982,2015,A1,.Locationinpatent:Paragraph0144;0146

[9]EuropeanJournalofMedicinalChemistry,2015,vol.95,p.174-184

[10]Patent:US2009/239848,2009,A1,.Locationinpatent:Page/Pagecolumn30

[11]DaltonTransactions,2017,vol.46,#35,p.11704-11714

[12]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[13]MedicinalChemistry,2016,vol.12,#5,p.489-498

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[15]Patent:CN108623537,2018,A,.Locationinpatent:Paragraph0087;0089

[16]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#9,p.1289-1298

[17]Patent:US2003/13708,2003,A1,

[18]Patent:US2004/87575,2004,A1,

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[1]OrganicLetters,2015,vol.17,#23,p.5934-5937

[2]OrganicLetters,2013,vol.15,#14,p.3734-3737

[1]OrganicLetters,2017,vol.19,#11,p.2809-2812

[1]JournalofMedicinalChemistry,2005,vol.48,#26,p.8261-8269

[2]BioorganicandMedicinalChemistryLetters,2004,vol.14,#5,p.1221-1227

[3]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2012,vol.51,#5,p.731-738

[4]BioorganicandMedicinalChemistryLetters,2012,vol.22,#13,p.4377-4385

[5]JournalofMedicinalChemistry,2012,vol.55,#23,p.10685-10699

[6]JournalofChemistry,2014,vol.2014,

[7]RSCAdvances,2015,vol.5,#113,p.93433-93437

[8]Patent:US2015/336982,2015,A1,

[9]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,#9,p.1289-1298

[10]Patent:CN106432239,2017,A,

[11]EuropeanJournalofMedicinalChemistry,2018,vol.155,p.303-315

[12]Patent:CN104583195,2018,B,

[13]Patent:US2013/45977,2013,A1,

[14]EuropeanJournalofMedicinalChemistry,2019,p.161-175

[15]EuropeanJournalofMedicinalChemistry,2019,p.690-709

[1]JournaloftheAmericanChemicalSociety,1948,vol.70,p.2223,2228

[2]JournaloftheAmericanChemicalSociety,1952,vol.74,p.2597,2599

[3]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[4]EuropeanJournalofMedicinalChemistry,2015,vol.95,p.174-184

[5]Patent:EP2949647,2015,A1,

[6]EuropeanJournalofMedicinalChemistry,2017,vol.125,p.1036-1050

[7]EuropeanJournalofMedicinalChemistry,2018,vol.158,p.593-619

[8]Patent:CN108623537,2018,A,

Downstream Synthesis Route

[1]AppliedOrganometallicChemistry,2018,vol.32

[2]BioorganicandMedicinalChemistry,2019,vol.27,p.1646-1657

[3]Patent:CN110818641,2020,A.Locationinpatent:Paragraph1019-1021;1026-1029

[4]Chemistry-AnAsianJournal,2017,vol.12,p.785-791

[5]BioorganicChemistry,2020,vol.98

[6]Patent:EP2949647,2015,A1.Locationinpatent:Paragraph0120

[7]EuropeanJournalofMedicinalChemistry,2016,vol.124,p.896-905

[8]Patent:EP3553065,2019,A1.Locationinpatent:Paragraph0124;0126

[9]Patent:CN110317176,2019,A.Locationinpatent:Paragraph0099;0102-0103

[10]BioorganicChemistry,2020,vol.95

[11]Patent:CN108707119,2018,A.Locationinpatent:Paragraph0066;0088;0089;0109;0110

[12]Patent:US2013/45977,2013,A1.Locationinpatent:Paragraph0215;0216;0217;0218

[13]RSCAdvances,2015,vol.5,p.93433-93437

[14]Patent:CN104583195,2018,B.Locationinpatent:Paragraph0486;0487;0491;0492;0493

[15]Patent:US2015/336982,2015,A1.Locationinpatent:Paragraph0144;0146

[16]EuropeanJournalofMedicinalChemistry,2015,vol.95,p.174-184

[17]Patent:KR101936851,2019,B1.Locationinpatent:Paragraph0348;0379-0382

[18]Patent:US2009/239848,2009,A1.Locationinpatent:Page/Pagecolumn30

[19]DaltonTransactions,2017,vol.46,p.11704-11714

[20]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[21]MedicinalChemistry,2016,vol.12,p.489-498

[22]EuropeanJournalofMedicinalChemistry,2020,vol.191

[23]Patent:CN108570012,2018,A.Locationinpatent:Paragraph0040;0044;0045

[24]Patent:CN108623537,2018,A.Locationinpatent:Paragraph0087;0089

[25]JournalofPolymerScience,PartA:PolymerChemistry,2016,vol.54,p.1289-1298

[26]Patent:US2003/13708,2003,A1

[27]Patent:US2004/87575,2004,A1

[28]Patent:US2004/110745,2004,A1

[29]Patent:CN106432239,2017,A.Locationinpatent:Paragraph0066;0077;0078

[30]CollectionofCzechoslovakChemicalCommunications,1986,vol.51,p.937-947

[31]JournalofChemistry,2014,vol.2014

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

[33]JournaloftheAmericanChemicalSociety,1948,vol.70,p.2223,2228

[34]JournaloftheAmericanChemicalSociety,1952,vol.74,p.2597,2599

[35]Patent:US2004763,1932,

[36]Patent:US2004763,1932,

[37]Patent:US2004763,1932,

[38]ActaChemicaScandinavica,1996,vol.50,p.1013-1019

[39]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.1221-1227

[40]JournalofMedicinalChemistry,2005,vol.48,p.8261-8269

[41]JournalofMedicinalChemistry,2008,vol.51,p.3507-3525

[42]JournalofMedicinalChemistry,2010,vol.53,p.4367-4378

[43]Patent:WO2007/64818,2007,A1.Locationinpatent:Page/Pagecolumn11-12

[44]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2012,vol.51,p.731-738

[45]BioorganicandMedicinalChemistryLetters,2012,vol.22,p.4377-4385

[46]JournalofMedicinalChemistry,2012,vol.55,p.10685-10699

[47]EuropeanJournalofMedicinalChemistry,2017,vol.125,p.1036-1050

[48]EuropeanJournalofMedicinalChemistry,2018,vol.155,p.303-315

[49]EuropeanJournalofMedicinalChemistry,2018,vol.158,p.593-619

[50]EuropeanJournalofMedicinalChemistry,2019,vol.162,p.161-175

[51]EuropeanJournalofMedicinalChemistry,2019,vol.163,p.690-709

[52]Patent:CN109678803,2019,A.Locationinpatent:Paragraph0223-0227

[53]NewJournalofChemistry,2019,vol.43,p.10190-10202

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[55]BioorganicChemistry,2020,vol.94

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[1]OrganicLetters,2003,vol.5,p.3515-3517

2524-67-6    555-57-7    33375-06-3   
C36H29IN2O6 
 
C63H58N6O7 

[1]Lo,MichaelM.-C.;Neumann,ChristopherS.;Nagayama,Satoshi;Perlstein,EthanO.;Schreiber,StuartL.[JournaloftheAmericanChemicalSociety,2004,vol.126,#49,p.16077-16086]

2524-67-6    483324-01-2   
N-(4-morpholin-4-ylphenyl)-4-(pyridin-3-yl)pyrimidin-2-amine 

[1]OrganicLetters,2005,vol.7,p.4113-4116

2524-67-6    15790-94-0   
EP7-229 

[1]Urbani,Paolo;Cavallo,Paolo;Cascio,MariaGrazia;Buonerba,Mariafrancesca;DeMartino,Giovanni;DiMarzo,Vincenzo;Saturnino,Carmela[BioorganicandMedicinalChemistryLetters,2006,vol.16,#1,p.138-141]

Literature

Title: Antistaphylococcal activity of DNA-interactive pyrrolobenzodiazepine (PBD) dimers and PBD-biaryl conjugates.

Journal: The Journal of antimicrobial chemotherapy 20120701

Title: 2,4-Diiodo-6-{[4-(morpholin-4-yl)phenyl]iminomethyl}phenol.

Journal: Acta crystallographica. Section E, Structure reports online 20110901

Title: 5-Meth-oxy-2-{[4-(morpholin-4-yl)phen-yl]imino-meth-yl}phenol.

Journal: Acta crystallographica. Section E, Structure reports online 20110901

Title: Synthesis and Pharmacological Evaluation of Novel Schiff Base Analogues of 3-(4-amino) Phenylimino) 5-fluoroindolin-2-one.

Journal: Journal of young pharmacists : JYP 20100101

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

Journal: Indian journal of pharmaceutical sciences 20090101

Title: Synthesis of Schiff bases of 4-(4-aminophenyl)-morpholine as potential antimicrobial agents.

Journal: European journal of medicinal chemistry 20050201

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