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22446-37-3,MFCD00090077
Catalog No.:AA0037GA

22446-37-3 | (2-Hydroxy-phenyl)-acetic acid methyl ester

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Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$14.00   $10.00
- +
5g
97%
in stock  
$17.00   $12.00
- +
10g
97%
in stock  
$22.00   $15.00
- +
25g
97%
in stock  
$41.00   $29.00
- +
100g
97%
in stock  
$151.00   $106.00
- +
  • 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:
AA0037GA
Chemical Name:
(2-Hydroxy-phenyl)-acetic acid methyl ester
CAS Number:
22446-37-3
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00090077
SMILES:
COC(=O)Cc1ccccc1O
Properties
Properties
 
BP:
261.9°C at 760 mmHg  
Form:
Solid  
MP:
122-124℃  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
156  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
1.2  

Upstream Synthesis Route

[1]Patent:US5922697,1999,A,

[1]OrganicandBiomolecularChemistry,2013,vol.11,#31,p.5147-5155

[2]JournalofMedicinalChemistry,2013,vol.56,#21,p.8948-8952

[3]OrganicLetters,2008,vol.10,#18,p.3969-3972

[4]Patent:WO2015/102990,2015,A1,.Locationinpatent:Paragraph0193-0195

[5]JournalofOrganicChemistry,1994,vol.59,#1,p.203-213

[6]EuropeanJournalofMedicinalChemistry,2009,vol.44,#4,p.1779-1787

[7]JournalofChemicalCrystallography,2009,vol.39,#12,p.927-930

[8]Patent:WO2018/93924,2018,A1,.Locationinpatent:Paragraph0313;0314

[9]Patent:WO2016/54728,2016,A1,.Locationinpatent:Paragraph00121

[10]Patent:WO2016/74068,2016,A1,.Locationinpatent:Paragraph00115

[11]JournalofMedicinalChemistry,2017,vol.60,#1,p.441-457

[12]JournaloftheAmericanChemicalSociety,1948,vol.70,p.1930

[13]JournaloftheAmericanChemicalSociety,1976,vol.98,p.3555-3564

[14]JournalofMedicinalChemistry,1968,vol.11,p.611-612

[15]Patent:WO2010/129379,2010,A1,.Locationinpatent:Page/Pagecolumn134

[16]Patent:WO2015/191616,2015,A1,.Locationinpatent:Paragraph0290

[17]Patent:JP5690514,2015,B2,.Locationinpatent:Paragraph0068

[18]Patent:TW2016/7949,2016,A,.Locationinpatent:Paragraph0066

[19]Patent:US2016/272650,2016,A1,.Locationinpatent:Paragraph0096-0097

[20]Patent:CN106380397,2017,A,.Locationinpatent:Paragraph0019;0020;0023;0024;0027;0028;0031;0032

[1]Patent:US5922697,1999,A,

[2]Patent:US4623652,1986,A,

[1]Patent:WO2003/99793,2003,A1,.Locationinpatent:Page247

[2]SyntheticCommunications,1994,vol.24,#19,p.2743-2747

[1]Patent:US5057146,1991,A,

[2]TetrahedronLetters,2013,vol.54,#37,p.5052-5055

Downstream Synthesis Route

[1]OrganicandBiomolecularChemistry,2013,vol.11,p.5147-5155

[2]JournalofMedicinalChemistry,2013,vol.56,p.8948-8952

[3]OrganicLetters,2008,vol.10,p.3969-3972

[4]Patent:WO2015/102990,2015,A1.Locationinpatent:Paragraph0193-0195

[5]JournalofOrganicChemistry,1994,vol.59,p.203-213

[6]EuropeanJournalofMedicinalChemistry,2009,vol.44,p.1779-1787

[7]Patent:WO2018/93924,2018,A1.Locationinpatent:Paragraph0313;0314

[8]Patent:WO2016/54728,2016,A1.Locationinpatent:Paragraph00121

[9]Patent:WO2016/74068,2016,A1.Locationinpatent:Paragraph00115

[10]JournalofMedicinalChemistry,2017,vol.60,p.441-457

[11]JournaloftheAmericanChemicalSociety,1948,vol.70,p.1930

[12]JournaloftheAmericanChemicalSociety,1976,vol.98,p.3555-3564

[13]Patent:WO2010/129379,2010,A1.Locationinpatent:Page/Pagecolumn134

[14]Patent:WO2015/191616,2015,A1.Locationinpatent:Paragraph0290

[15]Patent:JP5690514,2015,B2.Locationinpatent:Paragraph0068

[16]Patent:TW2016/7949,2016,A.Locationinpatent:Paragraph0066

[17]Patent:US2016/272650,2016,A1.Locationinpatent:Paragraph0096-0097

[18]Patent:CN106380397,2017,A.Locationinpatent:Paragraph0019;0020;0023;0024;0027;0028;0031;0032

[19]AngewandteChemie-InternationalEdition,2019,vol.58,p.7861-7865    Angew.Chem.,2019,vol.131,p.7943-7947,5

[20]JournalofMedicinalChemistry,1968,vol.11,p.611-612

[21]Patent:WO2019/199864,2019,A1.Locationinpatent:Paragraph0286;0287

[22]Organicandbiomolecularchemistry,2020,vol.18,p.1926-1932

[23]Chemistry-AEuropeanJournal,2020

[1]Patent:WO2003/99793,2003,A1.Locationinpatent:Page247

[2]SyntheticCommunications,1994,vol.24,p.2743-2747

[1]JournalofMedicinalChemistry,2004,vol.47,p.196-209

628329-89-5    22446-37-3   
2-(3-{3-propyl-1-5-(trifluoromethyl)-2-pyridyl-1H-pyrazol-4-yl}propoxy)phenylaceticacid 

[1]Patent:WO2003/99793,2003,A1.Locationinpatent:Page322

628329-91-9    22446-37-3   
2-(4-{3-propyl-1-5-(trifluoromethyl)-2-pyridinyl-1H-pyrazol-4-yl}butoxy)phenylaceticacid 

[1]Patent:WO2003/99793,2003,A1.Locationinpatent:Page330

Literature

Title: Synthesis, characterization and structure-activity relationship analysis of novel depsides as potential antibacterials.

Journal: European journal of medicinal chemistry 20090401

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SDS
Tags:22446-37-3 Molecular Formula|22446-37-3 MDL|22446-37-3 SMILES|22446-37-3 (2-Hydroxy-phenyl)-acetic acid methyl ester