Home Other Building Blocks 612-16-8
612-16-8,MFCD00004611
Catalog No.:AA0033AS

612-16-8 | 2-Methoxybenzyl alcohol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$16.00   $11.00
- +
25g
97%
in stock  
$35.00   $25.00
- +
100g
97%
in stock  
$119.00   $83.00
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500g
97%
in stock  
$482.00   $337.00
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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:
AA0033AS
Chemical Name:
2-Methoxybenzyl alcohol
CAS Number:
612-16-8
Molecular Formula:
C8H10O2
Molecular Weight:
138.1638
MDL Number:
MFCD00004611
SMILES:
COc1ccccc1CO
NSC Number:
66558
Properties
Properties
 
BP:
249°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.547(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
93.3  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
1.1  

Upstream Synthesis Route

[1]OrganicLetters,2002,vol.4,#12,p.2055-2058

[2]Tetrahedron,2008,vol.64,#7,p.1213-1217

[1]Tetrahedron,2006,vol.62,#42,p.9832-9839

[1]ChemistryLetters,1987,p.1113-1116

[1]ChemistryLetters,2013,vol.42,#9,p.1051-1052

[1]ChemistryLetters,2013,vol.42,#9,p.1051-1052

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2013,vol.135,p.10934-10937

[2]JournalofSteroidBiochemistryandMolecularBiology,2013,vol.137,p.332-344

[3]OrganicProcessResearchandDevelopment,2002,vol.6,p.190-191

[4]JournaloftheAmericanChemicalSociety,2013,vol.135,p.11951-11966

[5]AdvancedSynthesisandCatalysis,2010,vol.352,p.901-908

[6]OrganicLetters,2009,vol.11,p.469-472

[7]Synlett,2006,p.1965-1967

[8]JournalofHeterocyclicChemistry,1997,vol.34,p.835-844

[9]Patent:WO2020/84131,2020,A1.Locationinpatent:Page/Pagecolumn43

[10]MonatsheftefurChemie,1913,vol.34,p.1998

[11]JournalofMedicinalChemistry,1989,vol.32,p.1757-1763

[12]AngewandteChemie-InternationalEdition,2006,vol.45,p.606-609

[13]EuropeanJournalofOrganicChemistry,2007,p.1891-1904

[14]Chemistry-AEuropeanJournal,2008,vol.14,p.829-837

[15]TetrahedronLetters,2011,vol.52,p.13-16

[16]Organometallics,2011,vol.30,p.5493-5508

[17]JournaloftheAmericanChemicalSociety,2012,vol.134,p.9225-9239

[18]OrganicLetters,2013,vol.15,p.5818-5821

[19]Patent:EP3196191,2017,A1.Locationinpatent:Paragraph0040;0042

[20]AngewandteChemie-InternationalEdition,2017,vol.56,p.11807-11811    Angew.Chem.,2017,vol.129,p.11969-11973,5

[21]Biochemistry,2018,vol.57,p.2868-2875

[22]OrganicandBiomolecularChemistry,2018,vol.16,p.4304-4310

[1]Patent:WO2016/16238,2016,A1.Locationinpatent:Page/Pagecolumn105-106

[2]JournalofOrganicChemistry,1998,vol.63,p.9565-9568

[3]Synlett,2019,vol.30,p.943-946

[4]SyntheticCommunications,2018,vol.48,p.2793-2800

[5]SyntheticCommunications,1992,vol.22,p.1723-1734

[6]CollectionofCzechoslovakChemicalCommunications,1987,vol.52,p.2545-2563

[7]JournalofOrganicChemistry,1981,vol.46,p.2394-2398

[8]CanadianJournalofChemistry,1988,vol.66,p.1-10

[9]ChemischeBerichte,1992,vol.125,p.1061-1072

[10]JournaloftheAmericanChemicalSociety,2013,vol.135,p.1585-1592

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

[12]OrganicLetters,2015,vol.17,p.434-437

[13]ActaChemicaScandinavica(1947),1955,vol.9,p.555,560

[14]JournaloftheChemicalSociety,1954,p.1840,1841,1843

[15]CollectionofCzechoslovakChemicalCommunications,1964,vol.29,p.776-794

[16]JournaloftheChemicalSociety,1963,p.1947-1954

[17]JournalofOrganicChemistry,1992,vol.57,p.2865-2869

[18]PestManagementScience,2000,vol.56,p.875-881

[19]BioorganicandMedicinalChemistryLetters,2001,vol.11,p.2205-2208

[20]Patent:US5070089,1991,A

[21]OrganicLetters,2013,vol.15,p.108-111

[22]OrganicandBiomolecularChemistry,2013,vol.11,p.4016-4024

[23]JournalofOrganicChemistry,2019,vol.84,p.13252-13261

[24]Patent:US2019/330198,2019,A1.Locationinpatent:Paragraph0876

[1]Elangovan,Saravanakumar;Garbe,Marcel;Jiao,Haijun;Spannenberg,Anke;Junge,Kathrin;Beller,Matthias[AngewandteChemie-InternationalEdition,2016,vol.55,#49,p.15364-15368][Angew.Chem.,2016,#128,p.15590-15594]

[2]Oates,ConorL.;Widegren,MagnusB.;Clarke,MatthewL.[ChemicalCommunications,2020,vol.56,#61,p.8635-8638]

[3]Bagh,Bidraha;Behera,RakeshR.;Ghosh,Rahul;Khamari,Subrat;Panda,Surajit[OrganicLetters,2020,vol.22,#9,p.3642-3648]

[4]Bianco,A.;Passacantilli,P.;Righi,G.[SyntheticCommunications,1988,vol.18,#15,p.1765-1772]

[5]Prasanth;Joseph,Ebbin;Abhijith;Nair;Ibnusaud,Ibrahim;Raskatov,Jevgenij;Singaram,Bakthan[JournalofOrganicChemistry,2018,vol.83,#3,p.1431-1440]

[6]Schörgenhumer,Johannes;Zimmermann,Axel;Waser,Mario[OrganicProcessResearchandDevelopment,2018,vol.22,#7,p.862-870]

[7]Mozingo;Folkers[JournaloftheAmericanChemicalSociety,1948,vol.70,p.229]

[8]Kikugawa,Y.[Chemicalandpharmaceuticalbulletin,1976,vol.24,#5,p.1059-1063]

[9]Zanka,Atsuhiko;Ohmori,Hiroki;Okamoto,Takumi[Synlett,1999,#10,p.1636-1638]

[10]Higuchi,Takafumi;Tagawa,Risa;Iimuro,Atsuhiro;Akiyama,Shoko;Nagae,Haruki;Mashima,Kazushi[Chemistry-AEuropeanJournal,2017,vol.23,#52,p.12795-12804]

[11]Junge,Kathrin;Wendt,Bianca;Cingolani,Andrea;Spannenberg,Anke;Wei,Zhihong;Jiao,Haijun;Beller,Matthias[Chemistry-AEuropeanJournal,2018,vol.24,#5,p.1046-1052]

[12]Anaby,Aviel;Schelwies,Mathias;Schwaben,Jonas;Rominger,Frank;Hashmi,A.StephenK.;Schaub,Thomas[Organometallics,2018,vol.37,#13,p.2193-2201]

[13]Chakraborty,Soumi;Das,Arpan;Mandal,SwadhinK.[ChemicalCommunications,2021,vol.57,#94,p.12671-12674]

[1]Oates,ConorL.;Widegren,MagnusB.;Clarke,MatthewL.[ChemicalCommunications,2020,vol.56,#61,p.8635-8638]

[2]Holmberg[ActaChemicaScandinavica(1947),1955,vol.9,p.555,560]

[1]JustusLiebigsAnnalenderChemie,1977,p.2036-2066

Literature

Title: Intramolecular hydroxycarbene C-H-insertion: The curious case of (o-methoxyphenyl)hydroxycarbene.

Journal: Beilstein journal of organic chemistry 20100101

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