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55860-22-5,MFCD00095394
Catalog No.:AA00D8JJ

55860-22-5 | 2-Chloro-n-(2-methoxyphenyl)acetamide

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250mg
95%
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$21.00   $15.00
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1g
95%
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$72.00   $50.00
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10g
95%
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$258.00   $181.00
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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:
AA00D8JJ
Chemical Name:
2-Chloro-n-(2-methoxyphenyl)acetamide
CAS Number:
55860-22-5
Molecular Formula:
C9H10ClNO2
Molecular Weight:
199.6342
MDL Number:
MFCD00095394
SMILES:
ClCC(=O)Nc1ccccc1OC
NSC Number:
8284
Properties
Properties
 
BP:
339.0±22.0°C at 760 mmHg  
Form:
Solid  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
175  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
1.7  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2017,vol.60,#14,p.6289-6304

[2]BioorganicandMedicinalChemistry,2014,vol.22,#24,p.6885-6892

[3]Farmaco,2002,vol.57,#3,p.201-206

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2006,vol.45,#8,p.1871-1879

[5]BioorganicandMedicinalChemistry,2004,vol.12,#13,p.3471-3483

[6]Patent:US2003/232836,2003,A1,.Locationinpatent:Page47

[7]JournaloftheIndianChemicalSociety,1987,vol.64,#11,p.678-681

[8]Patent:US2008/221185,2008,A1,.Locationinpatent:Page/Pagecolumn23-24

[9]JournaloftheIranianChemicalSociety,2018,vol.15,#6,p.1261-1277

[10]ArchivderPharmazie,2013,vol.346,#11,p.793-804

[11]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1986,vol.25,p.438-440

[12]JournalofMedicinalChemistry,2012,vol.55,#14,p.6391-6402

[13]MedicinalChemistryResearch,2014,vol.23,#3,p.1290-1299

[14]JournaloftheAmericanChemicalSociety,1919,vol.41,p.1457

[15]ArchivderPharmazie(Weinheim,Germany),1915,vol.253,p.246

[16]JournalofBiologicalChemistry,1915,vol.21,p.150

[17]EuropeanJournalofMedicinalChemistry,1985,vol.20,#2,p.187-189

[18]ArchivderPharmazie,2004,vol.337,#2,p.105-111

[19]JournalofOrganicChemistry,2009,vol.74,#7,p.2846-2849

[20]BioorganicandMedicinalChemistryLetters,2010,vol.20,#9,p.2705-2708

[21]BioorganicandMedicinalChemistryLetters,2010,vol.20,#15,p.4661-4664

[22]ChemicalBiologyandDrugDesign,2011,vol.78,#2,p.309-313

[23]LettersinOrganicChemistry,2011,vol.8,#10,p.732-736

[24]BioorganicandMedicinalChemistryLetters,2012,vol.22,#15,p.5008-5012

[25]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2014,vol.53,#6,p.733-739

[26]BioorganicandMedicinalChemistry,2015,vol.23,#18,p.6173-6184

[27]ChemMedChem,2015,vol.10,#9,p.1489-1497

[28]JournalofHeterocyclicChemistry,2016,vol.53,#5,p.1595-1602

[29]EuropeanJournalofMedicinalChemistry,2016,vol.123,p.814-821

[30]MedicinalChemistry,2016,vol.12,#7,p.631-639

[31]ArchivderPharmazie,2016,vol.349,#11,p.864-880

[32]BioorganicChemistry,2018,vol.80,p.288-295

[33]JournalofHeterocyclicChemistry,2018,vol.55,#7,p.1756-1764

[34]ChemicalandPharmaceuticalBulletin,2017,vol.65,#10,p.950-958

[35]ChemistryandBiodiversity,2018,

[36]BioorganicandMedicinalChemistryLetters,2019,vol.29,#1,p.22-27

[1]Patent:US2004/29887,2004,A1,

[1]TetrahedronLetters,1999,vol.40,#49,p.8563-8566

[1]TetrahedronLetters,1999,vol.40,#49,p.8563-8566

[1]TetrahedronLetters,1999,vol.40,#49,p.8563-8566

Downstream Synthesis Route

[1]Zhukauskaite,L.N.;Tsybusov,A.P.;Gendenshtein,E.I.;Stankevichyus,A.P.;Tseplene,V.S.;Lubas,A.A.[PharmaceuticalChemistryJournal,1981,vol.15,#6,p.391-396][Khimiko-FarmatsevticheskiiZhurnal,1981,vol.15,#6,p.43-48]

[1]Murza,M.M.;Chuvyrov,A.N.;Zakirova,A.D.;Mukhamadiyarova,G.M.[JournalofOrganicChemistryUSSR(EnglishTranslation),1981,vol.17,#9,p.1750-1751][ZhurnalOrganicheskoiKhimii,1981,vol.17,#9,p.1961-1963]

[1]JournaloftheChemicalSociety,1955,p.739,743

[1]Locationinpatent:schemeortableSheng,Chunquan;Che,Xiaoying;Wang,Wenya;Wang,Shengzheng;Cao,Yongbing;Yao,Jianzhong;Miao,Zhenyuan;Zhang,Wannian[ChemicalBiologyandDrugDesign,2011,vol.78,#2,p.309-313]

[1]MedicinalChemistryResearch,2014,vol.23,p.1290-1299

Literature

Title: Discovery of novel N-phenylphenoxyacetamide derivatives as EthR inhibitors and ethionamide boosters by combining high-throughput screening and synthesis.

Journal: Journal of medicinal chemistry 20120726

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