Home Other Building Blocks 2480-86-6
2480-86-6,MFCD00238638
Catalog No.:AA002PEL

2480-86-6 | 4-(1-Hydroxyethyl)-2-methoxyphenol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$70.00   $49.00
- +
5g
98%
in stock  
$178.00   $125.00
- +
10g
98%
in stock  
$278.00   $195.00
- +
25g
98%
in stock  
$544.00   $381.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002PEL
Chemical Name:
4-(1-Hydroxyethyl)-2-methoxyphenol
CAS Number:
2480-86-6
Molecular Formula:
C9H12O3
Molecular Weight:
168.1898
MDL Number:
MFCD00238638
SMILES:
COc1cc(ccc1O)C(O)C
NSC Number:
47035
Properties
Properties
 
BP:
301.5°C at 760 mmHg  
Form:
Solid  
MP:
100-104°C(lit.);  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
138  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
0.4  

Downstream Synthesis Route

[1]Castellan,Alain;Grelier,Stephane;Kessab,Larbi;Nourmamode,Aziz;Hannachi,Yacine[JournaloftheChemicalSociety.PerkinTransactions2(2001),1996,vol.6,p.1131-1138]

[2]Wang,Ming-Hui;Chen,Ling-Yan[TetrahedronLetters,2017,vol.58,#8,p.732-735]

[3]Adler;Hernestam[ActaChemicaScandinavica(1947),1955,vol.9,p.319,332]

[4]Habu,Naoto;Samejima,Masahiro;Saburi,Yoshimasa;Yoshimoto,Tomataka[AgriculturalandBiologicalChemistry,1988,vol.52,#12,p.3073-3080]Takayama,Miyuki;Johjima,Toru;Yamanaka,Takeshi;Wariishi,Hiroyuki;Tanaka,Hiroo[SpectrochimicaActaPartA:MolecularandBiomolecularSpectroscopy,1997,vol.53,#10,p.1621-1628]

[5]Syrjänen,Kaisa;Brunow,Gösta[Tetrahedron,2001,vol.57,#2,p.365-370]

[6]Senohetal.[JournaloftheAmericanChemicalSociety,1959,vol.81,p.6240,6241]

[7]Locationinpatent:experimentalpartKumar,Prashant;Singh,AshishKumar;Yadav,Mahendra;Li,Pei-Zhou;Singh,SanjayKumar;Xu,Qiang;Pandey,DayaShankar[InorganicaChimicaActa,2011,vol.368,#1,p.124-131]

[8]Locationinpatent:schemeortableBogar,Krisztian;Krumlinde,Patrik;Bacsik,Zoltan;Hedin,Niklas;Baeckvall,Jan-E.[EuropeanJournalofOrganicChemistry,2011,#23,p.4409-4414]

[9]Meier,Sebastian;Riisager,Anders;Yang,Song;Zhao,Wenfeng[GreenChemistry,2020,vol.22,#18,p.5972-5977]

[1]Badamali,SushantaK.;Luque,Rafael;Clark,JamesH.;Breeden,SimonW.[CatalysisCommunications,2013,vol.31,p.1-4]

[2]Suri,O.P.;Bindra,R.S.;Satti,N.K.;Khajuria,R.K.[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1987,vol.26,#1-12,p.587-588]

[3]Habu,Naoto;Samejima,Masahiro;Saburi,Yoshimasa;Yoshimoto,Tomataka[AgriculturalandBiologicalChemistry,1988,vol.52,#12,p.3073-3080]

[4]Crestini,Claudia;Pastorini,Alessandra;Tagliatesta,Pietro[EuropeanJournalofInorganicChemistry,2004,#22,p.4477-4483]

[5]Jha,Ajay;Mhamane,Dattakumar;Suryawanshi,Anil;Joshi,SameerM.;Shaikh,Parvez;Biradar,Narayan;Ogale,Satishchandra;Rode,ChandrashekharV.[Catalysisscienceandtechnology,2014,vol.4,#6,p.1771-1778]

[6]CurrentPatentAssignee:NDSURESEARCHFOUNDATION-WO2017/156066,2017,A1Locationinpatent:Page/Pagecolumn35

[7]Song,Yang;Mobley,JustinK.;Motagamwala,AliHussain;Isaacs,Mark;Dumesic,JamesA.;Ralph,John;Lee,AdamF.;Wilson,Karen;Crocker,Mark[ChemicalScience,2018,vol.9,#42,p.8127-8133]

[1]SyntheticCommunications,1985,vol.15,p.1315-1324

[1]CollectionofCzechoslovakChemicalCommunications,1976,vol.41,p.299-310

[2]CollectionofCzechoslovakChemicalCommunications,1976,vol.41,p.299-310

2480-86-6    1197-09-7    121-33-5    139-85-5   
4-(1-hydroxy-ethyl)-1,2benzoquinone 

[1]Crestini,Claudia;Pastorini,Alessandra;Tagliatesta,Pietro[EuropeanJournalofInorganicChemistry,2004,#22,p.4477-4483]

Literature

Title: Decrease of 4-vinylguaiacol during beer aging and formation of apocynol and vanillin in beer.

Journal: Journal of agricultural and food chemistry 20081224

Title: Phenols and lignans from Chenopodium album.

Journal: Phytochemical analysis : PCA 20060101

Title: Cytotoxic terpenoid and immunosuppressive phenolic glycosides from the root bark of Dictamnus dasycarpus.

Journal: Planta medica 20020501

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