104-01-8,MFCD00004345
Catalog No.:AA003LLY

104-01-8 | 4-Methoxyphenylacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$6.00   $4.00
- +
25g
98%
in stock  
$7.00   $5.00
- +
100g
98%
in stock  
$26.00   $18.00
- +
500g
98%
in stock  
$83.00   $58.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003LLY
Chemical Name:
4-Methoxyphenylacetic acid
CAS Number:
104-01-8
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00004345
SMILES:
COc1ccc(cc1)CC(=O)O
UN Number:
3261
Properties
Properties
 
BP:
140°C at 760 mmHg  
Form:
Solid  
MP:
84-86 °C  
Refractive Index:
1.5101 (estimate)  
Solubility:
6g/l  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
148  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
1.4  

Upstream Synthesis Route

[1]ChemicalandPharmaceuticalBulletin,1998,vol.46,#4,p.581-586

[1]OrganicLetters,2006,vol.8,#24,p.5441-5443

[2]Tetrahedron,2012,vol.68,#26,p.5172-5178

[3]JournaloftheAmericanChemicalSociety,2012,vol.134,#44,p.18245-18248

[4]Tetrahedron,2018,vol.74,#16,p.2020-2029

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),2000,vol.4,p.567-570

[2]BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2962-2970

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1991,#12,p.3005-3008

[1]Patent:US2003/18193,2003,A1,

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1940,vol.5,p.606,608

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1942,vol.62,p.532;engl.Ref.S.169    Chem.Abstr.,1951,p.2861

[1]TetrahedronLetters,2018,vol.59,p.869-872

[2]Patent:US2012/225863,2012,A1.Locationinpatent:Page/Pagecolumn40-41

[3]MedicinalChemistryResearch,2012,vol.21,p.1313-1321

[4]Tetrahedron,2015,vol.71,p.9187-9195

[5]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1954,vol.74,p.495    Chem.Abstr.,1955,p.8182

[6]BioorganicandMedicinalChemistry,2008,vol.16,p.276-283

[7]ArchivderPharmazie,2010,vol.343,p.353-359

[8]Lettersindrugdesignanddiscovery,2011,vol.8,p.717-724

[9]MedicinalChemistryResearch,2014,vol.23,p.1465-1473

[10]MedicinalChemistryResearch,2020,vol.29,p.1520-1535

[1]JournalofOrganicChemistry,1970,vol.35,p.3596-3600

[1]Heterocycles,1990,vol.31,p.23-26

[2]Patent:CN103483210,2016,B.Locationinpatent:Paragraph0052;0053;0054

[3]ChemicalCommunications,2012,vol.48,p.10514-10516,3

[4]ChemicalandPharmaceuticalBulletin,1993,vol.41,p.2003-2006

[5]AustralianJournalofChemistry,1982,vol.35,p.1469-1480

[6]Synthesis,2011,p.1375-1382

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

[8]GreenChemistry,2013,vol.15,p.3020-3026

[9]Tetrahedron,2012,vol.68,p.7400-7407

[10]JournaloftheAmericanChemicalSociety,1967,vol.89,p.5259-5265

[11]BioorganicandMedicinalChemistryLetters,1999,vol.9,p.1619-1624

[12]HelveticaChimicaActa,1973,vol.56,p.2460-2479

[13]BulletinoftheChemicalSocietyofJapan,1987,vol.60,p.1091-1096

[14]JournaloftheAmericanChemicalSociety,1977,vol.99,p.3059-3067

[15]CanadianJournalofChemistry,1974,vol.52,p.749-760

[16]JournaloftheAmericanChemicalSociety,2008,vol.130,p.5206-5215

[17]Patent:WO2011/20193,2011,A1.Locationinpatent:Page/Pagecolumn25

[18]Synthesis,2011,p.2935-2940

[19]JournalofOrganicChemistry,2014,vol.79,p.11988-12003

[20]Chemistry-AEuropeanJournal,2015,vol.21,p.2785-2788

[21]AngewandteChemie-InternationalEdition,2015,vol.54,p.11240-11244    Angew.Chem.,2015,vol.127,p.11392-11396,5

[22]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.131-134

[23]BioorganicandMedicinalChemistry,2017,vol.25,p.3719-3735

[24]AngewandteChemie-InternationalEdition,2019,vol.58,p.9939-9943    Angew.Chem.,2019,vol.58,p.10044-10048,5

Literature

Title: Ester and carbamate ester derivatives of Biochanin A: synthesis and in vitro evaluation of estrogenic and antiproliferative activities.

Journal: Bioorganic & medicinal chemistry 20120501

Title: Evaluation of (R)-(-)-α-methoxy phenyl acetic acid as a chiral shift reagent for resolution and determination of R and S enantiomers of modafinil in bulk drugs and formulations by 1H NMR spectroscopy.

Journal: Chirality 20120401

Title: Biological evaluation of phenolic constituents from the trunk of Berberis koreana.

Journal: Bioorganic & medicinal chemistry letters 20110415

Title: 2-(3-Bromo-4-meth-oxy-phen-yl)acetic acid.

Journal: Acta crystallographica. Section E, Structure reports online 20100701

Title: Anticancer activity of dinuclear gallium(III) carboxylate complexes.

Journal: European journal of medicinal chemistry 20100201

Title: Characterization of pu-erh tea using chemical and metabolic profiling approaches.

Journal: Journal of agricultural and food chemistry 20090422

Title: Coenzyme Q0 induces apoptosis and modulates the cell cycle in estrogen receptor negative breast cancer cells.

Journal: Anti-cancer drugs 20090101

Title: Study of the cytotoxic activity of di and triphenyltin(IV) carboxylate complexes.

Journal: Journal of inorganic biochemistry 20081201

Title: 1-(2-Hydr-oxy-3,4-dimethoxy-phen-yl)-2-(4-methoxy-phen-yl)ethanone.

Journal: Acta crystallographica. Section E, Structure reports online 20081201

Title: Lipophilic (hydroxy)phenylacetates by solvent-free lipase-catalyzed esterification and transesterification in vacuo.

Journal: Journal of agricultural and food chemistry 20080709

Title: Biotransformation of p-methoxyphenylacetonitrile into p-methoxyphenylacetic acid by resting cells of Bacillus subtilis.

Journal: Biotechnology and applied biochemistry 20080701

Title: 15N CIDNP investigations of the peroxynitric acid nitration of L-tyrosine and of related compounds.

Journal: Organic & biomolecular chemistry 20060221

Title: Effect of applied potential on arylmethyl films oxidatively grafted to carbon surfaces.

Journal: Langmuir : the ACS journal of surfaces and colloids 20051122

Title: Contribution of aldehyde oxidase, xanthine oxidase, and aldehyde dehydrogenase on the oxidation of aromatic aldehydes.

Journal: Chemical research in toxicology 20041001

Title: Development and substantiation of a liquid chromatographic method for monitoring organic reactions involved in synthesis of 4-methoxyphenylacetic acid.

Journal: Journal of chromatography. A 20021004

Title: Fine structural specificity differences of trimethoprim allergenic determinants.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 19961001

Title: Xiang C, et al. Cortisol, cortisone, and 4-methoxyphenylacetic acid as potential plasma biomarkers for early detection of non-small cell lung cancer. Int J Biol Markers. 2018 Aug;33(3):314-320.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:104-01-8 Molecular Formula|104-01-8 MDL|104-01-8 SMILES|104-01-8 4-Methoxyphenylacetic acid
Catalog No.: AA003LLY
104-01-8,MFCD00004345
104-01-8 | 4-Methoxyphenylacetic acid
Pack Size: 10g
Purity: 98%
in stock
$6.00 $4.00
Pack Size: 25g
Purity: 98%
in stock
$7.00 $5.00
Pack Size: 100g
Purity: 98%
in stock
$26.00 $18.00
Pack Size: 500g
Purity: 98%
in stock
$83.00 $58.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003LLY
Chemical Name: 4-Methoxyphenylacetic acid
CAS Number: 104-01-8
Molecular Formula: C9H10O3
Molecular Weight: 166.1739
MDL Number: MFCD00004345
SMILES: COc1ccc(cc1)CC(=O)O
UN Number: 3261
Properties
BP: 140°C at 760 mmHg  
Form: Solid  
MP: 84-86 °C  
Refractive Index: 1.5101 (estimate)  
Solubility: 6g/l  
Storage: Keep in dry area;Room Temperature;  
Complexity: 148  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 1.4  
Upstream Synthesis Route
104-01-8    10338-51-9 

[1]ChemicalandPharmaceuticalBulletin,1998,vol.46,#4,p.581-586

104-01-8    531-95-3 

[1]OrganicLetters,2006,vol.8,#24,p.5441-5443

[2]Tetrahedron,2012,vol.68,#26,p.5172-5178

[3]JournaloftheAmericanChemicalSociety,2012,vol.134,#44,p.18245-18248

[4]Tetrahedron,2018,vol.74,#16,p.2020-2029

104-01-8    491-80-5 

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),2000,vol.4,p.567-570

[2]BioorganicandMedicinalChemistry,2012,vol.20,#9,p.2962-2970

104-01-8    108-73-6    491-80-5 

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1991,#12,p.3005-3008

104-01-8    13435-12-6    7087-68-5 

[1]Patent:US2003/18193,2003,A1,

Downstream Synthesis Route
6343-93-7    104-01-8 

[1]JournalofOrganicChemistry,1940,vol.5,p.606,608

104-01-8    77287-34-4    6343-93-7 

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1942,vol.62,p.532;engl.Ref.S.169    Chem.Abstr.,1951,p.2861

104-01-8    100-66-3    120-44-5 

[1]TetrahedronLetters,2018,vol.59,p.869-872

[2]Patent:US2012/225863,2012,A1.Locationinpatent:Page/Pagecolumn40-41

[3]MedicinalChemistryResearch,2012,vol.21,p.1313-1321

[4]Tetrahedron,2015,vol.71,p.9187-9195

[5]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1954,vol.74,p.495    Chem.Abstr.,1955,p.8182

[6]BioorganicandMedicinalChemistry,2008,vol.16,p.276-283

[7]ArchivderPharmazie,2010,vol.343,p.353-359

[8]Lettersindrugdesignanddiscovery,2011,vol.8,p.717-724

[9]MedicinalChemistryResearch,2014,vol.23,p.1465-1473

[10]MedicinalChemistryResearch,2020,vol.29,p.1520-1535

1849-54-3    104-01-8    25957-08-8 

[1]JournalofOrganicChemistry,1970,vol.35,p.3596-3600

104-01-8    702-23-8 

[1]Heterocycles,1990,vol.31,p.23-26

[2]Patent:CN103483210,2016,B.Locationinpatent:Paragraph0052;0053;0054

[3]ChemicalCommunications,2012,vol.48,p.10514-10516,3

[4]ChemicalandPharmaceuticalBulletin,1993,vol.41,p.2003-2006

[5]AustralianJournalofChemistry,1982,vol.35,p.1469-1480

[6]Synthesis,2011,p.1375-1382

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

[8]GreenChemistry,2013,vol.15,p.3020-3026

[9]Tetrahedron,2012,vol.68,p.7400-7407

[10]JournaloftheAmericanChemicalSociety,1967,vol.89,p.5259-5265

[11]BioorganicandMedicinalChemistryLetters,1999,vol.9,p.1619-1624

[12]HelveticaChimicaActa,1973,vol.56,p.2460-2479

[13]BulletinoftheChemicalSocietyofJapan,1987,vol.60,p.1091-1096

[14]JournaloftheAmericanChemicalSociety,1977,vol.99,p.3059-3067

[15]CanadianJournalofChemistry,1974,vol.52,p.749-760

[16]JournaloftheAmericanChemicalSociety,2008,vol.130,p.5206-5215

[17]Patent:WO2011/20193,2011,A1.Locationinpatent:Page/Pagecolumn25

[18]Synthesis,2011,p.2935-2940

[19]JournalofOrganicChemistry,2014,vol.79,p.11988-12003

[20]Chemistry-AEuropeanJournal,2015,vol.21,p.2785-2788

[21]AngewandteChemie-InternationalEdition,2015,vol.54,p.11240-11244    Angew.Chem.,2015,vol.127,p.11392-11396,5

[22]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.131-134

[23]BioorganicandMedicinalChemistry,2017,vol.25,p.3719-3735

[24]AngewandteChemie-InternationalEdition,2019,vol.58,p.9939-9943    Angew.Chem.,2019,vol.58,p.10044-10048,5

Literature fold

Title: Ester and carbamate ester derivatives of Biochanin A: synthesis and in vitro evaluation of estrogenic and antiproliferative activities.

Journal: Bioorganic & medicinal chemistry20120501

Title: Evaluation of (R)-(-)-α-methoxy phenyl acetic acid as a chiral shift reagent for resolution and determination of R and S enantiomers of modafinil in bulk drugs and formulations by 1H NMR spectroscopy.

Journal: Chirality20120401

Title: Biological evaluation of phenolic constituents from the trunk of Berberis koreana.

Journal: Bioorganic & medicinal chemistry letters20110415

Title: 2-(3-Bromo-4-meth-oxy-phen-yl)acetic acid.

Journal: Acta crystallographica. Section E, Structure reports online20100701

Title: Anticancer activity of dinuclear gallium(III) carboxylate complexes.

Journal: European journal of medicinal chemistry20100201

Title: Characterization of pu-erh tea using chemical and metabolic profiling approaches.

Journal: Journal of agricultural and food chemistry20090422

Title: Coenzyme Q0 induces apoptosis and modulates the cell cycle in estrogen receptor negative breast cancer cells.

Journal: Anti-cancer drugs20090101

Title: Study of the cytotoxic activity of di and triphenyltin(IV) carboxylate complexes.

Journal: Journal of inorganic biochemistry20081201

Title: 1-(2-Hydr-oxy-3,4-dimethoxy-phen-yl)-2-(4-methoxy-phen-yl)ethanone.

Journal: Acta crystallographica. Section E, Structure reports online20081201

Title: Lipophilic (hydroxy)phenylacetates by solvent-free lipase-catalyzed esterification and transesterification in vacuo.

Journal: Journal of agricultural and food chemistry20080709

Title: Biotransformation of p-methoxyphenylacetonitrile into p-methoxyphenylacetic acid by resting cells of Bacillus subtilis.

Journal: Biotechnology and applied biochemistry20080701

Title: 15N CIDNP investigations of the peroxynitric acid nitration of L-tyrosine and of related compounds.

Journal: Organic & biomolecular chemistry20060221

Title: Effect of applied potential on arylmethyl films oxidatively grafted to carbon surfaces.

Journal: Langmuir : the ACS journal of surfaces and colloids20051122

Title: Contribution of aldehyde oxidase, xanthine oxidase, and aldehyde dehydrogenase on the oxidation of aromatic aldehydes.

Journal: Chemical research in toxicology20041001

Title: Development and substantiation of a liquid chromatographic method for monitoring organic reactions involved in synthesis of 4-methoxyphenylacetic acid.

Journal: Journal of chromatography. A20021004

Title: Fine structural specificity differences of trimethoprim allergenic determinants.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology19961001

Title: Xiang C, et al. Cortisol, cortisone, and 4-methoxyphenylacetic acid as potential plasma biomarkers for early detection of non-small cell lung cancer. Int J Biol Markers. 2018 Aug;33(3):314-320.

Building Blocks More >
622-52-6
622-52-6
1-(4-Methylphenyl)-2-thiourea
AA003LPQ | MFCD00041190
77359-11-6
77359-11-6
Mono-4-nitrobenzyl malonate
AA003LSL | MFCD00191556
537-47-3
537-47-3
4-Phenylsemicarbazide
AA003LWS | MFCD00007590
694521-58-9
694521-58-9
5-(2,4-Dichlorophenyl)-3-(3-nitrophenyl)-1,2,4-oxadiazole
AA003M0I | MFCD03717917
4272-77-9
4272-77-9
Dansyl acid
AA003M4K | MFCD00003995
786643-20-7
786643-20-7
D149 Dye
AA003M8A | MFCD13184819
87905-98-4
87905-98-4
5-Amino-N-benzyloxycarbonylpentanol
AA003MBM | MFCD01863135
868066-91-5
868066-91-5
5-Bromo-2-methylisoindolin-1-one
AA003MEZ | MFCD12755780
3884-71-7
3884-71-7
5-Bromo-pentan-2-one
AA003MI2 | MFCD00051425
1131-17-5
1131-17-5
5-Chloro-3-methyl-1-phenylpyrazole
AA003ML8 | MFCD00067853
Submit
© 2017 AA BLOCKS, INC. All rights reserved.