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1485-07-0,MFCD00004128
Catalog No.:AA001KW1

1485-07-0 | 2-Naphthaleneethanol

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Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$46.00   $32.00
- +
1g
95%
in stock  
$57.00   $40.00
- +
5g
95%
in stock  
$195.00   $137.00
- +
25g
95%
in stock  
$507.00   $355.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001KW1
Chemical Name:
2-Naphthaleneethanol
CAS Number:
1485-07-0
Molecular Formula:
C12H12O
Molecular Weight:
172.2231
MDL Number:
MFCD00004128
SMILES:
OCCc1ccc2c(c1)cccc2
NSC Number:
21040
Properties
Properties
 
BP:
309.8°C at 760 mmHg  
Form:
Solid  
MP:
66-68 °C(lit.)  
Refractive Index:
1.5340 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
155  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
3.2  

Downstream Synthesis Route

[1]Novak,Lajos;Rohaly,Janos;Poppe,Laszlo;Hornyanszky,Gabor;Kolonits,Pal;etal.[LiebigsAnnalenderChemie,1992,#2,p.145-158]

[2]Banks,TonyM.;Clay,SamuelF.;Glover,StephenA.;Schumacher,RhiannonR.[OrganicandBiomolecularChemistry,2016,vol.14,#15,p.3699-3714]

[3]Nishizawa,Seiichi;Cui,Ying-Yu;Minagawa,Masakazu;Morita,Kotaro;Kato,Yuichi;Taniguchi,Shinichiro;Kato,Ryo;Teramae,Norio[JournaloftheChemicalSociety.PerkinTransactions2(2001),2002,#5,p.866-870]

[4]CurrentPatentAssignee:NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH;CENTRENATIONALDELARECHERCHESCIENTIFIQUE;QUANTUMGENOMICS;COLLEGEDEFRANCE-WO2020/84131,2020,A1Locationinpatent:Page/Pagecolumn70

[5]CurrentPatentAssignee:NOVOGENLTD-WO2016/8011,2016,A1Locationinpatent:Page/Pagecolumn58;59

[6]Tatewosjan;Babajan[ZhurnalObshcheiKhimii,1952,vol.22,p.1421,1426;engl.Ausg.S.1465,1469]

[7]Karreretal.[HelveticaChimicaActa,1940,vol.23,p.585,586]

[8]Cagniant,P.etal.[BulletindelaSocieteChimiquedeFrance,1961,p.1934-1937]Campaigne,E.;Heaton,B.G.[JournalofOrganicChemistry,1964,vol.29,p.2372-2378]

[9]Mitra,A.K.etal.[JournaloftheIndianChemicalSociety,1971,vol.48,p.391-394]

[10]CurrentPatentAssignee:PFIZERINC-US4644071,1987,A

[1]CurrentPatentAssignee:NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH;CENTRENATIONALDELARECHERCHESCIENTIFIQUE;QUANTUMGENOMICS;COLLEGEDEFRANCE-WO2020/84131,2020,A1Locationinpatent:Page/Pagecolumn69

[2]Banks,TonyM.;Clay,SamuelF.;Glover,StephenA.;Schumacher,RhiannonR.[OrganicandBiomolecularChemistry,2016,vol.14,#15,p.3699-3714]

[3]Mayr,Stefanie;Marin-Luna,Marta;Zipse,Hendrik[JournalofOrganicChemistry,2021,vol.86,#4,p.3456-3489]

[4]Locationinpatent:experimentalpartMorales-Serna,JoseAntonio;Garcia-Rios,Erendira;Bernal,Jorge;Paleo,Ehecatl;Gavino,Ruben;Cardenas,Jorge[Synthesis,2011,#9,p.1375-1382]

[5]Nishizawa,Seiichi;Cui,Ying-Yu;Minagawa,Masakazu;Morita,Kotaro;Kato,Yuichi;Taniguchi,Shinichiro;Kato,Ryo;Teramae,Norio[JournaloftheChemicalSociety.PerkinTransactions2(2001),2002,#5,p.866-870]

[6]Lawesson[ActaChemicaScandinavica(1947),1958,vol.12,p.1,7]

[7]Schadt,F.L.etal.[JournaloftheAmericanChemicalSociety,1978,vol.100,p.228-246]

[8]Mitra,A.K.etal.[JournaloftheIndianChemicalSociety,1971,vol.48,p.391-394]Liang,Jiang-Lin;Yuan,Shi-Xue;Huang,Jie-Sheng;Che,Chi-Ming[JournalofOrganicChemistry,2004,vol.69,#11,p.3610-3619]

[9]Campaigne,E.;Heaton,B.G.[JournalofOrganicChemistry,1964,vol.29,p.2372-2378]

[10]Gilbert,Andrew;Heath,Peter;Kashoulis-Koupparis,Annoula;Ellis-Davies,GrahamC.R.;Firth,SusanM.[JournaloftheChemicalSociety.PerkintransactionsI,1988,p.31-36]

[11]CurrentPatentAssignee:MERCK&COINC-WO2006/52555,2006,A2Locationinpatent:Page/Pagecolumn26;40-41

[12]Revelant,Germain;Dunand,Sandrine;Hesse,Stephanie;Kirsch,Gilbert[Synthesis,2011,#18,p.2935-2940]

[13]Maity,Prantik;Srinivas,HarathiD.;Watson,MaryP.[JournaloftheAmericanChemicalSociety,2011,vol.133,#43,p.17142-17145]

[14]CurrentPatentAssignee:GILEADSCIENCESINC-US2013/123231,2013,A1Locationinpatent:Paragraph1262;1263;1264

[15]Gising,Johan;Belfrage,AnnaKarin;Alogheli,Hiba;Ehrenberg,Angelica;Åkerblom,Eva;Svensson,Richard;Artursson,Per;Karlén,Anders;Danielson,U.Helena;Larhed,Mats;Sandström,Anja[JournalofMedicinalChemistry,2014,vol.57,#5,p.1790-1801]

[16]CurrentPatentAssignee:ROCHEHOLDINGAG;PARAZAPHARMAINC-WO2018/96159,2018,A1Locationinpatent:Paragraph0261-0264

[17]Kojima,Masahiro;Matsunaga,Shigeki[Synthesis,2020,vol.52,#13,p.1934-1946]

110-87-2    1485-07-0   
2-(2-Naphthalen-2-yl-ethoxy)-tetrahydro-pyran 

[1]Olah,GeorgeA.;Husain,Altaf;Singh,BrijP.[Synthesis,1983,#11,p.892-895]

358-23-6    1485-07-0   
Trifluoro-methanesulfonicacid2-naphthalen-2-yl-ethylester 

[1]Berkowitz,DavidB.;Eggen,MariJean;Shen,Quanrong;Sloss,DarbyG.[JournalofOrganicChemistry,1993,vol.58,#23,p.6174-6176]

[2]Mallick,Shubhadip;Würthwein,Ernst-Ulrich;Studer,Armido[OrganicLetters,2020,vol.22,#16,p.6568-6572]

[1]Park,TaeKyo;Schroeder,Joseph;RebekJr.,Julius[Tetrahedron,1991,vol.47,#14-15,p.2507-2518]

[2]Askew;Ballester;Buhr;Jeong;Jones;Parris;Williams;RebekJr.[JournaloftheAmericanChemicalSociety,1989,vol.111,#3,p.1082-1090]

Literature

Title: The role of weak hydrogen bonds in chiral recognition.

Journal: Physical chemistry chemical physics : PCCP 20111028

Title: Intra- vs. intermolecular hydrogen bonding: dimers of alpha-hydroxyesters with methanol.

Journal: Physical chemistry chemical physics : PCCP 20061014

Title: Chiral recognition between lactic acid derivatives and an aromatic alcohol in a supersonic expansion: electronic and vibrational spectroscopy.

Journal: Physical chemistry chemical physics : PCCP 20060227

Title: Chemoenzymatic synthesis of optically active, biodegradable polymers based on phenyl- and naphthyl-ethanols esterified with divinyladipate.

Journal: Biotechnology letters 20040401

Title: Resolution of 1-(2-naphthyl)ethanol by a combination of an enzyme-catalyzed kinetic resolution with a fluorous triphasic separative reaction.

Journal: Organic letters 20020725

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Tags:1485-07-0 Molecular Formula|1485-07-0 MDL|1485-07-0 SMILES|1485-07-0 2-Naphthaleneethanol