Home Other Building Blocks 569-42-6
569-42-6,MFCD00042701
Catalog No.:AA0032KS

569-42-6 | 1,8-Naphthalenediol

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Purity
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1g
98%
in stock  
$46.00   $32.00
- +
5g
95%
in stock  
$74.00   $52.00
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10g
95%
in stock  
$116.00   $81.00
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25g
98%
in stock  
$218.00   $153.00
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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:
AA0032KS
Chemical Name:
1,8-Naphthalenediol
CAS Number:
569-42-6
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
MDL Number:
MFCD00042701
SMILES:
Oc1cccc2c1c(O)ccc2
Properties
Properties
 
BP:
375.4 °C at 760 mmHg  
Form:
Solid  
MP:
142-143 °C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
142  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
XLogP3:
2.8  

Upstream Synthesis Route

[1]TurkishJournalofChemistry,2018,vol.42,#5,p.1398-1407

[2]OrganicLetters,2011,vol.13,#17,p.4494-4497

[3]Patent:WO2017/205350,2017,A1,.Locationinpatent:Page/Pagecolumn21

[4]JournalofOrganicChemistry,1986,vol.51,#22,p.4291-4294

[5]HuaxueXuebao,1958,vol.24,p.311,317

[6]Chem.Abstr.,1959,p.19989

[1]AngewandteChemie-InternationalEdition,2010,vol.49,#30,p.5146-5150

[2]Patent:WO2011/103442,2011,A2,.Locationinpatent:Page/Pagecolumn7;65-66

[3]HelveticaChimicaActa,1921,vol.4,p.341

[4]Journalofmedicinalchemistry,1971,vol.14,#11,p.1023-1026

[1]RecueildesTravauxChimiquesdesPays-Bas,1939,vol.58,p.125,130,131

[1]JournaloftheChemicalSociety,1956,p.2412,2415

[1]TurkishJournalofChemistry,2018,vol.42,#5,p.1398-1407

[2]JournaloftheChemicalSociety,1956,p.2412,2415

[3]HelveticaChimicaActa,1950,vol.33,p.595,596

[4]JournalofOrganicChemistry,1980,vol.45,#6,p.1149-1151

Downstream Synthesis Route

[1]Hashemi;Akhbari[RussianJournalofOrganicChemistry,2005,vol.41,#6,p.935-936]

[2]Llopis,Natalia;Baeza,Alejandro[JournalofOrganicChemistry,2020,vol.85,#9,p.6159-6164]

[3]Teuber;Goetz[ChemischeBerichte,1954,vol.87,p.1236,1250]

[4]Erdmann[JustusLiebigsAnnalenderChemie,1888,vol.247,p.359]

[5]Willstaetter;Wheeler[ChemischeBerichte,1914,vol.47,p.2799]

[6]Jiang,Jia-Heng;Boominathan,SivaSenthilKumar;Hu,Wan-Ping;Chen,Chung-Yu;Vandavasi,JayaKishore;Lin,Ying-Ting;Wang,Jeh-Jeng[EuropeanJournalofOrganicChemistry,2016,vol.2016,#13,p.2284-2289]

[1]Parada,GiovannyA.;Glover,StarlaD.;Orthaber,Andreas;Hammarström,Leif;Ott,Sascha[EuropeanJournalofOrganicChemistry,2016,vol.2016,#20,p.3365-3372]

[2]CurrentPatentAssignee:TONGJIUNIVERSITY-WO2021/114313,2021,A1Locationinpatent:Page/Pagecolumn53;54

[3]Zhu,Zhongwei;Koltunov,KonstantinYu.[MendeleevCommunications,2016,vol.26,#1,p.78-80]

[4]CurrentPatentAssignee:NANJINGKEFEIPINGSHENGHUIPHARMACY-CN109111418,2019,ALocationinpatent:Paragraph0121-0128

[5]Chen,Lei;Su,Mei;Jin,Qiu;Wang,Wei;Wang,Chun-Gu;Assani,Israa;Wang,Mu-Xuan;Zhao,Shi-Feng;Lv,Shen-Min;Wang,Jia-Wei;Sun,Bo;Li,Yan;Liao,Zhi-Xin[JournalofMedicinalChemistry,2021,vol.64,#21,p.16106-16131]

[6]Assani,Israa;Chen,Lei;Huang,Ri-Zhen;Jin,Qiu;Kang,Yang-yang;Li,Yan;Liao,Zhi-Xin;Lv,Shen-Min;Su,Mei;Sun,Bo;Wang,Chun-Gu;Wang,De-Zhong;Wang,Jia-Wei;Wang,Mu-Xuan;Wu,Xian-Zhi;Zhao,Shi-Feng[EuropeanJournalofMedicinalChemistry,2022,vol.229]

[7]Assani,Israa;Chen,Lei;Huang,Ri-Zhen;Jin,Qiu;Kang,Yang-yang;Li,Yan;Liao,Zhi-Xin;Lv,Shen-Min;Su,Mei;Sun,Bo;Wang,Chun-Gu;Wang,De-Zhong;Wang,Jia-Wei;Wang,Mu-Xuan;Wu,Xian-Zhi;Zhao,Shi-Feng[EuropeanJournalofMedicinalChemistry,2022,vol.229]

[8]Hochsteinetal.[JournaloftheAmericanChemicalSociety,1953,vol.75,p.5455,5474]

[1]Bahramnezhad,Baharak;Ghazanfari,Dadkhoda;Sheikhhosseini,Enayatollah;Akhgar,MohammadReza;Ahmadi,SayedAli[JournalofHeterocyclicChemistry,2020,vol.57,#1,p.173-181]

[2]Perekalin;Padwa[ZhurnalObshcheiKhimii,1957,vol.27,p.2578,2582,2583;engl.Ausg.S.2635,2638,2639]

[3]Buu-Hoi;Lavit[JournaloftheChemicalSociety,1956,p.2412,2415]

[1]Snyder,ScottA.;Sherwood,TrevorC.;Ross,AudreyG.[AngewandteChemie-InternationalEdition,2010,vol.49,#30,p.5146-5150]

[2]CurrentPatentAssignee:COLUMBIAUNIVERSITYINTHECITYOFNEWYORK-WO2011/103442,2011,A2Locationinpatent:Page/Pagecolumn7;65-66

[3]Staudinger;Schlenker;Goldstein[HelveticaChimicaActa,1921,vol.4,p.341]

[4]Jorgensen;Slade[Journalofmedicinalchemistry,1971,vol.14,#11,p.1023-1026]

[1]Turkmen,YunusEmre[TurkishJournalofChemistry,2018,vol.42,#5,p.1398-1407]

[2]Buu-Hoi;Lavit[JournaloftheChemicalSociety,1956,p.2412,2415]Schmidetal.[HelveticaChimicaActa,1950,vol.33,p.595,596]

[3]Parker;Iqbal[JournalofOrganicChemistry,1980,vol.45,#6,p.1149-1151]

Literature

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Title: ChLae1 and ChVel1 regulate T-toxin production, virulence, oxidative stress response, and development of the maize pathogen Cochliobolus heterostrophus.

Journal: PLoS pathogens 20120201

Title: Naphthol radical couplings determine structural features and enantiomeric excess of dalesconols in Daldinia eschscholzii.

Journal: Nature communications 20120101

Title: Physicochemical characterization and antioxidant activity of melanin from a novel strain of Aspergillus bridgeri ICTF-201.

Journal: Letters in applied microbiology 20110901

Title: Terpenoid and phenolic metabolites from the fungus xylaria sp. associated with termite nests.

Journal: Chemistry & biodiversity 20110901

Title: Characterization of a polyketide synthase in Aspergillus niger whose product is a precursor for both dihydroxynaphthalene (DHN) melanin and naphtho-γ-pyrone.

Journal: Fungal genetics and biology : FG & B 20110401

Title: Conidial Dihydroxynaphthalene Melanin of the Human Pathogenic Fungus Aspergillus fumigatus Interferes with the Host Endocytosis Pathway.

Journal: Frontiers in microbiology 20110101

Title: Identification and characterization of an Aspergillus fumigatus 'supermater' pair.

Journal: mBio 20110101

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Journal: Chemistry & biodiversity 20101201

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Journal: Current genetics 20100801

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Journal: Journal of enzyme inhibition and medicinal chemistry 20091201

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Journal: Microbes and infection 20090401

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Journal: BMC microbiology 20090101

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Title: Adaptation of extremely halotolerant black yeast Hortaea werneckii to increased osmolarity: a molecular perspective at a glance.

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Journal: FEMS microbiology letters 20071001

Title: A trinucleating ligand based on 1,8-naphthalenediol: synthesis, structural and magnetic properties of a linear Cu(II)Cu(II)Cu(II) complex.

Journal: Chemical communications (Cambridge, England) 20070128

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Journal: PloS one 20070101

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Tags:569-42-6 Molecular Formula|569-42-6 MDL|569-42-6 SMILES|569-42-6 1,8-Naphthalenediol |Organic_Building_Blocks