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569-42-6 | Naphthalene-1,8-diol
CAS No: 569-42-6 Catalog No: AG0032NK MDL No:MFCD00042701
Product Description
Catalog Number:
AG0032NK
Chemical Name:
Naphthalene-1,8-diol
CAS Number:
569-42-6
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
MDL Number:
MFCD00042701
IUPAC Name:
naphthalene-1,8-diol
InChI:
InChI=1S/C10H8O2/c11-8-5-1-3-7-4-2-6-9(12)10(7)8/h1-6,11-12H
InChI Key:
OENHRRVNRZBNNS-UHFFFAOYSA-N
SMILES:
Oc1cccc2c1c(O)ccc2
EC Number:
209-316-5
Properties
Complexity:
142
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
160.052g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
160.172g/mol
Monoisotopic Mass:
160.052g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8
Literature
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|---|---|
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| Melanin is an essential component for the integrity of the cell wall of Aspergillus fumigatus conidia. | BMC microbiology 20090101 |
| New biosynthetic step in the melanin pathway of Wangiella (Exophiala) dermatitidis: evidence for 2-acetyl-1,3,6,8-Tetrahydroxynaphthalene as a novel precursor. | Eukaryotic cell 20081001 |
| Adaptation of extremely halotolerant black yeast Hortaea werneckii to increased osmolarity: a molecular perspective at a glance. | Studies in mycology 20080101 |
| Regulation of melanin biosynthesis via the dihydroxynaphthalene pathway is dependent on sexual development in the ascomycete Sordaria macrospora. | FEMS microbiology letters 20071001 |
| A trinucleating ligand based on 1,8-naphthalenediol: synthesis, structural and magnetic properties of a linear Cu(II)Cu(II)Cu(II) complex. | Chemical communications (Cambridge, England) 20070128 |
| Ionizing radiation changes the electronic properties of melanin and enhances the growth of melanized fungi. | PloS one 20070101 |
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| Ferromagnetic coupling by orthogonal magnetic orbitals in a heterodinuclear CuIIVIV=O complex and in a homodinuclear CuIICuII complex. | Inorganic chemistry 20060626 |
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| Effects of disrupting the polyketide synthase gene WdPKS1 in Wangiella [Exophiala] dermatitidis on melanin production and resistance to killing by antifungal compounds, enzymatic degradation, and extremes in temperature. | BMC microbiology 20060101 |
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| Identification of 1,8-dihydroxynaphthalene melanin in Monosporascus cannonballus and the analysis of hexaketide and pentaketide compounds produced by wild-type and pigmented isolates of the fungus. | Journal of agricultural and food chemistry 20040630 |
| Evidence for 1,8-dihydroxynaphthalene melanin in three halophilic black yeasts grown under saline and non-saline conditions. | FEMS microbiology letters 20040319 |
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| clap1, a gene encoding a copper-transporting ATPase involved in the process of infection by the phytopathogenic fungus Colletotrichum lindemuthianum. | Molecular genetics and genomics : MGG 20021001 |
| 1,8-Dihydroxynaphthalene monoglucoside, a new metabolite of Sclerotinia sclerotiorum, and the effect of tricyclazole on its production. | Canadian journal of microbiology 20020401 |
| The role of melanin in the antagonistic interaction between the apple scab pathogen Venturia inaequalis and Microsphaeropsis ochracea. | Canadian journal of microbiology 20020401 |
| Localization of melanin in conidia of Alternaria alternata using phage display antibodies. | Molecular plant-microbe interactions : MPMI 20020301 |
| Pentaketide melanin biosynthesis in Aspergillus fumigatus requires chain-length shortening of a heptaketide precursor. | The Journal of biological chemistry 20010803 |
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