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581-43-1,MFCD00004082
Catalog No.:AA00359F

581-43-1 | 2,6-Dihydroxynaphthalene

Pack Size
Purity
Availability
Price(USD)
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250mg
98%
in stock  
$6.00   $4.00
- +
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$32.00   $22.00
- +
10g
98%
in stock  
$55.00   $39.00
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100g
98%
in stock  
$426.00   $298.00
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500g
98%
in stock  
$1,575.00   $1,103.00
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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:
AA00359F
Chemical Name:
2,6-Dihydroxynaphthalene
CAS Number:
581-43-1
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
MDL Number:
MFCD00004082
SMILES:
Oc1ccc2c(c1)ccc(c2)O
NSC Number:
62687
Properties
Properties
 
BP:
246.06°C (rough estimate)  
Form:
Solid  
MP:
223 - 225 C (Decomposes)  
Refractive Index:
1.5418 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
140  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
XLogP3:
2.3  

Upstream Synthesis Route

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1994,#8,p.1055-1060

[1]TetrahedronLetters,1983,vol.24,#30,p.3099-3102

[2]TetrahedronLetters,1983,vol.24,#30,p.3099-3102

[1]CanadianJournalofChemistry,1987,vol.65,p.2397-2404

[2]CrystEngComm,2017,vol.19,#11,p.1464-1469

[3]ChineseJournalofChemistry,2017,vol.35,#8,p.1289-1293

[4]JournalofOrganicChemistry,2016,vol.81,#19,p.8744-8758

[5]JournalofChemicalResearch,2012,vol.36,#11,p.675-677

[1]IsraelJournalofChemistry,2014,vol.54,#5-6,p.796-816

[2]ChemischeBerichte,1907,vol.40,p.1413

[3]JournalofMedicinalChemistry,1993,vol.36,#20,p.2891-2898

[4]BulletinoftheChemicalSocietyofJapan,1989,vol.62,#2,p.545-550

[5]JournalofMedicinalChemistry,2007,vol.50,#22,p.5293-5300

[6]JournalofMedicinalChemistry,2012,vol.55,#12,p.5720-5733

[1]Tetrahedron,1982,vol.38,#15,p.2347-2354

[2]Patent:US6365775,2002,B1,.Locationinpatent:Pagecolumn11

Downstream Synthesis Route

[1]ChemischeBerichte,1903,vol.36,p.570

581-43-1    88-45-9   
2-amino-5-(6-hydroxy-2naphthylamino)-benzenesulfonicacid 

[1]Patent:DE291021,    Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.12,p.541

[1]Patent:TWI617564,2018,B.Locationinpatent:Paragraph0017;0019;0020

[2]JournalofOrganicChemistry,2010,vol.75,p.1228-1234

[3]Patent:US2011/224445,2011,A1.Locationinpatent:Page/Pagecolumn15

[4]Patent:KR2016/83235,2016,A.Locationinpatent:Paragraph0070-0073

[5]Patent:US2020/16151,2020,A1.Locationinpatent:Paragraph0775;0835-0837

[6]ChemischeBerichte,1907,vol.40,p.3975

[7]ChemicalCommunications,2012,vol.48,p.573-575

[8]Organicelectronics,2012,vol.13,p.3183-3194

[9]JournalofPolymerScience,PartA:PolymerChemistry,2013,vol.51,p.2948-2958

[10]Patent:US9127020,2015,B2.Locationinpatent:Page/Pagecolumn25

[11]DyesandPigments,2017,vol.137,p.117-125

[12]DyesandPigments,2019,vol.163,p.30-39

[1]Patent:US10174043,2019,B1.Locationinpatent:Page/Pagecolumn15

[2]Patent:WO2019/23022,2019,A1.Locationinpatent:Paragraph0034

[3]TetrahedronLetters,1998,vol.39,p.6487-6490

[4]Patent:WO2013/149001,2013,A2.Locationinpatent:Paragraph00123

[5]JournaloftheChemicalSociety,1937,p.1859,1861

[6]Patent:US2011/224445,2011,A1.Locationinpatent:Page/Pagecolumn8

[1]ChemicalCommunications,2017,vol.53,p.9616-9619

[2]ZhurnalObshcheiKhimii,1935,vol.5,p.877,881    ChemischesZentralblatt,1936,vol.107,p.2935

[3]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.1391-1393

[4]OrganicandBiomolecularChemistry,2019,vol.17,p.3971-3977

[5]Patent:CN110642677,2020,A.Locationinpatent:Paragraph0048-0050

Literature

Title: A light-controlled molecular brake with complete ON-OFF rotation.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20100315

Title: Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives.

Journal: The Journal of organic chemistry 20100219

Title: New thermal and microbial resistant metal-containing epoxy polymers.

Journal: Bioinorganic chemistry and applications 20100101

Title: Chromane derivatives of small aromatic molecules: Chemoenzymatic synthesis and growth inhibitory activity on human tumor cell line LoVo WT.

Journal: Bioorganic & medicinal chemistry 20090815

Title: Experimental and theoretical studies on constitutional isomers of 2,6-dihydroxynaphthalene carbaldehydes. Effects of resonance-assisted hydrogen bonding on the electronic absorption spectra.

Journal: The Journal of organic chemistry 20090116

Title: 4,4'-(2,6-Dihydroxy-naphthalene-1,5-diyldimethyl-ene)dipyridinium bis-(per-chlorate).

Journal: Acta crystallographica. Section E, Structure reports online 20080601

Title: Toward high-generation rotaxane dendrimers that incorporate a ring component on every branch: noncovalent synthesis of a dendritic [10]pseudorotaxane with 13 molecular components.

Journal: Chemistry, an Asian journal 20070604

Title: Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides.

Journal: Journal of medicinal chemistry 20060323

Title: The influence of aromatic residues in hydraphile spacer units: assay by ion selective electrode methods and in bacteria.

Journal: Bioorganic & medicinal chemistry 20050502

Title: Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase.

Journal: Biochemistry 20050412

Title: Regiospecific oxidation of naphthalene and fluorene by toluene monooxygenases and engineered toluene 4-monooxygenases of Pseudomonas mendocina KR1.

Journal: Biotechnology and bioengineering 20050405

Title: Oxidase enzyme immobilisation through electropolymerised films to assemble biosensors for batch and flow injection analysis.

Journal: Biosensors & bioelectronics 20030501

Title: Novel solid-state polycondensation I. Oxidative-coupling polymerization of 2,6-dihydroxynaphthalene.

Journal: Chemical communications (Cambridge, England) 20020121

Title: A covalent vanadium(III) 2-dimensional network and vanadyl chains linked by aryldioxides.

Journal: Inorganic chemistry 20010115

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