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1877-75-4,MFCD00014360
Catalog No.:AA003LLD

1877-75-4 | 4-Methoxyphenoxyacetic acid

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Purity
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250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
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5g
97%
in stock  
$23.00   $16.00
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25g
97%
in stock  
$50.00   $35.00
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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:
AA003LLD
Chemical Name:
4-Methoxyphenoxyacetic acid
CAS Number:
1877-75-4
Molecular Formula:
C9H10O4
Molecular Weight:
182.1733
MDL Number:
MFCD00014360
SMILES:
COc1ccc(cc1)OCC(=O)O
Properties
Properties
 
BP:
328°C at 760 mmHg  
Form:
Solid  
MP:
112-114 °C  
Refractive Index:
1.4345 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
161  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
1.2  

Upstream Synthesis Route

[1]Patent:WO2003/93258,2003,A2,.Locationinpatent:Page/Pagecolumn18

[1]SyntheticCommunications,1996,vol.26,#23,p.4337-4341

[2]JournalofFluorescence,2015,vol.25,#4,p.849-859

[3]Luminescence,2018,vol.33,#5,p.855-862

[4]Luminescence,2015,vol.30,#5,p.677-685

[5]JournalofMolecularStructure,2014,vol.1074,p.487-495

[6]JournaloftheIndianChemicalSociety,1991,vol.68,#3,p.135-137

[7]Tetrahedron,2004,vol.60,#46SPEC.ISS.,p.10469-10477

[8]JournaloftheAmericanChemicalSociety,1931,vol.53,p.304

[9]JournaloftheAmericanChemicalSociety,1943,vol.65,p.1555

[10]ChimicaTherapeutica,1970,vol.5,p.211-215

[11]AgriculturalandBiologicalChemistry,1983,vol.47,#11,p.2653-2656

[12]BioorganicandMedicinalChemistryLetters,2008,vol.18,#16,p.4597-4601

[13]EuropeanJournalofMedicinalChemistry,2009,vol.44,#11,p.4726-4733

[14]BioorganicandMedicinalChemistry,2014,vol.22,#12,p.3180-3186

[15]Phosphorus,SulfurandSiliconandtheRelatedElements,2014,vol.189,#9,p.1337-1345

[16]ResearchonChemicalIntermediates,2016,vol.42,#6,p.5269-5280

[17]JournalofHeterocyclicChemistry,2016,vol.53,#1,p.183-187

[18]Patent:CN103666452,2016,B,.Locationinpatent:Paragraph0076;0077

[1]MedicinalChemistryResearch,2010,vol.19,#1,p.33-57

[2]DyesandPigments,2018,vol.158,p.28-35

[3]Luminescence,2014,vol.29,#8,p.1113-1122

[1]JournalofMaterialsChemistry,1998,vol.8,#4,p.919-924

[2]JournaloftheAmericanChemicalSociety,1987,vol.109,p.5235

[3]BioorganicandMedicinalChemistry,2008,vol.16,#23,p.10049-10060

[4]BritishJournalofPharmacology,2013,vol.170,#4,p.822-834

[5]Patent:WO2014/100730,2014,A1,.Locationinpatent:Paragraph00270

[6]BioorganicandMedicinalChemistryLetters,2016,vol.26,#10,p.2526-2530

[1]JournaloftheAmericanChemicalSociety,1987,vol.109,p.5235

[2]BritishJournalofPharmacology,2013,vol.170,#4,p.822-834

[3]Chemistry-AEuropeanJournal,2014,vol.20,#18,p.5492-5500

[4]Patent:WO2014/100730,2014,A1,

[5]BioorganicandMedicinalChemistryLetters,2014,vol.24,#16,p.3732-3735

[6]BioorganicandMedicinalChemistryLetters,2015,vol.25,#23,p.5601-5603

[7]BioorganicandMedicinalChemistryLetters,2016,vol.26,#10,p.2526-2530

Downstream Synthesis Route

[1]Villemin,Didier;Hammadi,Mohamed[SyntheticCommunications,1996,vol.26,#23,p.4337-4341]

[2]Yan,Dong;Li,Dong;Cheng,Guang;Yang,Zehui;Shi,Ling;Guo,Dongcai[JournalofFluorescence,2015,vol.25,#4,p.849-859]

[3]Wu,Yongqiang;Guo,Tiantong;Shu,Dehua;Zhang,Wu;Luan,Fangfei;Shi,Ling;Guo,Dongcai[Luminescence,2018,vol.33,#5,p.855-862]

[4]Xiao,Haihua;Jiang,Xi;Li,Dong;Wu,Limin;Zhang,Wu;Guo,Dongcai[Luminescence,2015,vol.30,#5,p.677-685]

[5]Yan,Dong;Xiang,Yu;Li,Kangyun;Chen,Yanwen;Yang,Zehui;Guo,Dongcai[JournalofMolecularStructure,2014,vol.1074,p.487-495]

[6]Sharma;Rani;Talwar;Kalsi[JournaloftheIndianChemicalSociety,1991,vol.68,#3,p.135-137]

[7]Huang,Wei;Song,Yuming;Wang,Jing;Cao,Guoying;Zheng,Zhuo[Tetrahedron,2004,vol.60,#46SPEC.ISS.,p.10469-10477]

[8]Koelsch[JournaloftheAmericanChemicalSociety,1931,vol.53,p.304]Hayes;Branch[JournaloftheAmericanChemicalSociety,1943,vol.65,p.1555]

[9]Maccari,M.etal.[ChimicaTherapeutica,1970,vol.5,p.211-215]

[10]Hayashi,Masatoshi;Wada,Kojiro;Munakata,Katsura[AgriculturalandBiologicalChemistry,1983,vol.47,#11,p.2653-2656]

[11]Locationinpatent:bodytextKhanum,ShaukathAra;Khanum,NoorFatima;Shashikanth[BioorganicandMedicinalChemistryLetters,2008,vol.18,#16,p.4597-4601]

[12]Locationinpatent:schemeortableYu,Zhiyi;Shi,Guanying;Sun,Qiu;Jin,Hong;Teng,Yun;Tao,Ke;Zhou,Guoping;Liu,Wei;Wen,Fang;Hou,Taiping[EuropeanJournalofMedicinalChemistry,2009,vol.44,#11,p.4726-4733]

[13]He,Jun-Bo;Ren,Yan-Liang;Sun,Qiu-Shuang;You,Ge-Yun;Zhang,Li;Zou,Peng;Feng,Ling-Ling;Wan,Jian;He,Hong-Wu[BioorganicandMedicinalChemistry,2014,vol.22,#12,p.3180-3186]

[14]Hu,Bing;Zhai,Yue-Yuan;Zhang,Ling;Zhang,You-Ming;Wei,Tai-Bao[Phosphorus,SulfurandSiliconandtheRelatedElements,2014,vol.189,#9,p.1337-1345]Meng,Defen;Xu,De;Li,Dong;Dai,Ming;Li,Guizhi;Guo,Dongcai[ResearchonChemicalIntermediates,2016,vol.42,#6,p.5269-5280]

[15]Mo,Wenyan;Shi,Yanxia;He,Junbo;Li,Baoju;Peng,Hao;He,Hongwu[JournalofHeterocyclicChemistry,2016,vol.53,#1,p.183-187]

[16]CurrentPatentAssignee:SUNYAT-SENUNIVERSITY(CHINA)-CN103666452,2016,BLocationinpatent:Paragraph0076;0077

[1]Bhat;Bhat;Shenoy[JournalofPharmacyandPharmacology,2001,vol.53,#2,p.267-272]

[2]Yan,Dong;Li,Dong;Cheng,Guang;Yang,Zehui;Shi,Ling;Guo,Dongcai[JournalofFluorescence,2015,vol.25,#4,p.849-859]

[3]Xiao,Haihua;Jiang,Xi;Li,Dong;Wu,Limin;Zhang,Wu;Guo,Dongcai[Luminescence,2015,vol.30,#5,p.677-685]

[4]Wu,Yongqiang;Guo,Tiantong;Shu,Dehua;Zhang,Wu;Luan,Fangfei;Shi,Ling;Guo,Dongcai[Luminescence,2018,vol.33,#5,p.855-862]

[5]Zhu,Jian-Jun;Wang,Pei-Yi;Long,Zhou-Qing;Xiang,Shu-Zhen;Zhang,Jun-Rong;Li,Zhen-Xing;Wu,Yuan-Yuan;Shao,Wu-Bin;Zhou,Xiang;Liu,Li-Wei;Yang,Song[JournalofAgriculturalandFoodChemistry,2022,vol.70,#9,p.2825-2838]

1877-75-4    2065-37-4   
2-bromo-3-(4-methoxyphenoxymethyl)-1,4-naphthoquinone 

[1]Tetrahedron,2003,vol.59,p.5941-5946

[1]Khalafi-Nezhad,Ali;Parhami,Abolfath;SoltaniRad,MohammadNavid;Zarea,Abdolkarim[TetrahedronLetters,2005,vol.46,#40,p.6879-6882]

[1]JournalofOrganicChemistry,2002,vol.67,p.4458-4465

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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