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61266-36-2,MFCD00168848
Catalog No.:AA00EBM6

61266-36-2 | Methyl 4-(3-hydroxyprop-1-ynyl)benzoate

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Purity
Availability
Price(USD)
Quantity
  
250mg
in stock  
$104.00   $73.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
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  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00EBM6
Chemical Name:
Methyl 4-(3-hydroxyprop-1-ynyl)benzoate
CAS Number:
61266-36-2
Molecular Formula:
C11H10O3
Molecular Weight:
190.1953
MDL Number:
MFCD00168848
SMILES:
OCC#Cc1ccc(cc1)C(=O)OC
Properties
Properties
 
Form:
Solid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
250  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
1.8  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,1997,vol.40,#16,p.2502-2524

Downstream Synthesis Route

[1]Synthesis,1984,vol.NO.9,p.728-729

[2]DokladyChemistry,1985,vol.283,p.212-214    Dokl.Akad.NaukSSSRSer.Khim.,1985,vol.283,p.630-633

[1]BioorganicandMedicinalChemistryLetters,1996,vol.6,p.473-476

[2]JournalofMedicinalChemistry,1997,vol.40,p.2502-2524

[3]JournalofOrganicChemistry,1992,vol.57,p.5757-5761

[4]Patent:US5426110,1995,A

[5]Patent:CN103254083,2016,B.Locationinpatent:Paragraph0265-0268

[1]CrystalGrowthandDesign,2017,vol.17,p.3665-3676

[2]ChemicalCommunications,2017,vol.53,p.4681-4684

[3]Synthesis,1984,vol.NO.9,p.728-729

[4]DokladyChemistry,1985,vol.283,p.212-214    Dokl.Akad.NaukSSSRSer.Khim.,1985,vol.283,p.630-633

[5]Patent:CN103254083,2016,B.Locationinpatent:Paragraph0265-0268

[1]BulletinoftheAcademyofSciencesoftheUSSRDivisionofChemicalScience,1984,vol.33,p.1433-1438    IzvestiyaAkademiiNaukSSSR,SeriyaKhimicheskaya,1984,p.1561-1566

[2]Tetrahedron,2018,vol.74,p.3578-3588

[3]BioorganicandMedicinalChemistryLetters,1996,vol.6,p.473-476

[4]Synthesis,1984,vol.NO.9,p.728-729

[5]DokladyChemistry,1985,vol.283,p.212-214    Dokl.Akad.NaukSSSRSer.Khim.,1985,vol.283,p.630-633

[6]AdvancedSynthesisandCatalysis,2020,vol.362,p.146-151

[7]Chemistry-AEuropeanJournal,2014,vol.20,p.13894-13900

[8]JournalofMedicinalChemistry,1997,vol.40,p.2502-2524

[9]JournalofOrganicChemistry,1992,vol.57,p.5757-5761

[10]EuropeanJournalofOrganicChemistry,2018,vol.2018,p.4900-4904

[11]Organometallics,2016,vol.35,p.816-826

[12]JournaloftheAmericanChemicalSociety,2017,vol.139,p.8114-8117

[13]BioorganicandMedicinalChemistryLetters,2014,vol.24,p.1550-1556

[14]Chemistry-AEuropeanJournal,2017,vol.23,p.15332-15335

[15]Patent:US2002/65308,2002,A1

[16]JournaloftheAmericanChemicalSociety,2010,vol.132,p.11440-11442

[17]Chemistry-AEuropeanJournal,2014,vol.20,p.5910-5913

[18]AdvancedSynthesisandCatalysis,2016,vol.358,p.1571-1576

[19]JournaloftheAmericanChemicalSociety,2016,vol.138,p.12073-12076

[20]AngewandteChemie-InternationalEdition,2017,vol.56,p.9868-9871    Angew.Chem.,2017,vol.129,p.10000-10003,4

[21]JournalofOrganicChemistry,2019,vol.84,p.1630-1639

[22]OrganicLetters,2019,vol.21,p.8308-8311

[23]OrganicandBiomolecularChemistry,2019,vol.17,p.8737-8744

[24]Organicandbiomolecularchemistry,2020,vol.18,p.3374-3381

[25]AngewandteChemie-InternationalEdition,2020,vol.59,p.11010-11019    Angew.Chem.,2020,vol.132,p.11103-11112,10

619-44-3   
C7H9CuO2 
  61266-36-2 

[1]JournaloftheChemicalSociety.PerkintransactionsI,1976,p.1612-1615

Literature
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