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4670-10-4,MFCD00016827
Catalog No.:AA003ILC

4670-10-4 | 3,5-Dimethoxyphenylacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
95%
in stock  
$18.00   $13.00
- +
5g
97%
in stock  
$23.00   $16.00
- +
10g
97%
in stock  
$28.00   $20.00
- +
25g
97%
in stock  
$68.00   $48.00
- +
100g
97%
in stock  
$271.00   $190.00
- +
  • 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:
AA003ILC
Chemical Name:
3,5-Dimethoxyphenylacetic acid
CAS Number:
4670-10-4
Molecular Formula:
C10H12O4
Molecular Weight:
196.1999
MDL Number:
MFCD00016827
SMILES:
COc1cc(CC(=O)O)cc(c1)OC
Properties
Properties
 
BP:
352.6 °C at 760 mmHg  
Form:
Solid  
MP:
102-103 °C(lit.);  
Refractive Index:
1.5430 (estimate)  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
1.3  

Upstream Synthesis Route

[1]TetrahedronLetters,2018,vol.59,#17,p.1670-1673

[2]JournalofMedicinalChemistry,2013,vol.56,#24,p.10142-10157

[3]ACSMedicinalChemistryLetters,2016,vol.7,#4,p.424-428

[1]Patent:WO2014/144737,2014,A1,.Locationinpatent:Paragraph00718

[2]JournalofMedicinalChemistry,1984,vol.27,#2,p.190-195

[3]MedChemComm,2013,vol.4,#2,p.332-339

[4]ChineseJournalofChemistry,2010,vol.28,#6,p.1041-1043

[1]Patent:US6255301,2001,B1,

Downstream Synthesis Route

[1]TetrahedronLetters,1994,vol.35,p.1367-1370

[2]AdvancedSynthesisandCatalysis,2007,vol.349,p.583-594

[3]JournalofMedicinalChemistry,2013,vol.56,p.10142-10157

[4]JournalofOrganicChemistry,1952,vol.17,p.568,570

[5]AustralianJournalofChemistry,1953,vol.6,p.373

[6]Tetrahedron,1962,vol.18,p.1519-1526

[7]HelveticaChimicaActa,1963,vol.46,p.1358-1360

[8]ChemistryandPhysicsofLipids,1995,vol.78,p.29-36

[9]JournaloftheAmericanChemicalSociety,2004,vol.126,p.5942-5943

[10]JournalofOrganicChemistry,2020,vol.85,p.4103-4113

[1]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.3613-3621

[2]JournaloftheAmericanChemicalSociety,2018,vol.140,p.5065-5068

[3]TetrahedronLetters,1994,vol.35,p.1367-1370

[4]JournalofOrganicChemistry,2020,vol.85,p.4103-4113

[5]Patent:WO2013/83991,2013,A1.Locationinpatent:Page/Pagecolumn71

[6]JournalofMedicinalChemistry,2014,vol.57,p.2773-2788

[7]OrganicandBiomolecularChemistry,2016,vol.14,p.7468-7479

[8]Synthesis,2010,p.1550-1556

[9]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.756-760

[10]JournaloftheAmericanChemicalSociety,1956,vol.78,p.4801,4805

[11]Patent:US2003/176498,2003,A1

[12]Patent:WO2015/106108,2015,A2.Locationinpatent:Paragraph0272-0273

[13]AngewandteChemie-InternationalEdition,2015,vol.54,p.13357-13361    Angew.Chem.,2015,vol.127,p.13555-13559,5

[14]ACSMedicinalChemistryLetters,2016,vol.7,p.424-428

[15]Patent:US2016/311769,2016,A1.Locationinpatent:Paragraph0311-0312

[1]BioorganicandMedicinalChemistry,2012,vol.20,p.4862-4871

[2]JournalofOrganicChemistry,1952,vol.17,p.568,570

[1]Liang,Qiren;Zhang,Jiyong;Quan,Weiguo;Sun,Yongquan;She,Xuegong;Pan,Xinfu[JournalofOrganicChemistry,2007,vol.72,#7,p.2694-2697]

[2]DellaVolpe;Linciano;Listro;Tumminelli;Amadio;Bonomo;Elgaher;Adam;Hirsch;Boeckler;Vasile;Rossi;Collina[BioorganicChemistry,2021,vol.116]

[3]Baker,P.M.etal.[JournaloftheChemicalSocietyC:Organic,1967,p.1913-1915]

[4]Wasserman,H.H.;Gambale,R.J.[TetrahedronLetters,1981,vol.22,#48,p.4849-4852]

[5]Stone,MartinJ.;Maplestone,RachaelA.;Man,ShirleyK.Rah;Williams,DudneyH.[TetrahedronLetters,1991,vol.32,#23,p.2663-2666]

[6]Piettre,Arnaud;Chevenier,Emmanuel;Massardier,Christine;Gimbert,Yves;Greene,AndrewE.[OrganicLetters,2002,vol.4,#18,p.3139-3142]

[1]Patent:WO2014/144737,2014,A1.Locationinpatent:Paragraph00718

[2]JournalofMedicinalChemistry,1984,vol.27,p.190-195

[3]MedChemComm,2013,vol.4,p.332-339

[4]ChineseJournalofChemistry,2010,vol.28,p.1041-1043

Literature

Title: Efficient synthesis of natural polyphenolic stilbenes: resveratrol, piceatannol and oxyresveratrol.

Journal: Chemical & pharmaceutical bulletin 20101101

Title: Methyl 3,5-dibromo-4-methyl-benzoate.

Journal: Acta crystallographica. Section E, Structure reports online 20100401

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