1,6-Dihydroxy Naphthalene

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Product Information

Molecular Formula:
C10H8O2
Molecular Weight:
160.17
Description
Naphthalene-1,6-diol is a naphthalenediol.
Synonyms
1,6-NAPHTHALENEDIOL; 1,6-DIHYDROXYNAPHTHALENE; 2,5-DIHYDROXYNAPHTHALENE; 2,5-Naphthalenediol; 6-Hydroxy-1-naphthol; C.I. 76630
IUPAC Name
naphthalene-1,6-diol
Canonical SMILES
C1=CC2=C(C=CC(=C2)O)C(=C1)O
InChI
InChI=1S/C10H8O2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6,11-12H
InChI Key
FZZQNEVOYIYFPF-UHFFFAOYSA-N
Boiling Point
375.4°C at 760 mmHg
Melting Point
130-133°C
Purity
98%
Density
1.33 g/cm3
Appearance
prisms
Storage
Keep away from heat, sparks, and flame.

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

XLogP3
1.9
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
160.052429494 g/mol
Monoisotopic Mass
160.052429494 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
158
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
JP-2022040214-A Resin composition 2022-01-05
JP-2022028036-A Dry films, cured products, and electronic components 2021-12-21
JP-2022031285-A Resin composition, sheet-like laminated material, printed wiring board and semiconductor device 2021-11-24
CN-114011242-A Carboxylated poly (arylene ether nitrile) ultrafiltration membrane and preparation method thereof 2021-11-22
JP-2022022261-A Resin composition 2021-11-22
JP-2022027768-A Resin composition 2021-11-16
CN-114163463-A Near-infrared fluorescent two-photon fluorescent probe design aiming at real-time change of hydrogen peroxide in tumor process and synthetic method thereof 2021-10-31
CN-113929846-A High-carbon-formation-rate water-soluble phenolic resin and preparation method thereof 2021-10-22
CN-113861383-A Epoxy resin containing naphthalene ring structure and preparation method thereof 2021-10-19
JP-2022017350-A Adhesive sheet with support 2021-10-19

Literatures

PMID Publication Date Title Journal
23016299 2012-06-01 [Simultaneous determination of seven naphthalenediols in cosmetics by reversed-phase high performance liquid chromatography] Se pu = Chinese journal of chromatography
21217882 2010-09-01 Various aspects of piscine toxicology Interdisciplinary toxicology
18682327 2008-09-01 Chemoenzymatic syntheses of prenylated aromatic small molecules using Streptomyces prenyltransferases with relaxed substrate specificities Bioorganic & medicinal chemistry
17609576 2007-07-01 Naphthalene-1,6-diol: a three-dimensional framework built from O-H...O, O-H...pi and C-H...O hydrogen bonds Acta crystallographica. Section C, Crystal structure communications
17260959 2007-02-06 Understanding the substrate selectivity and the product regioselectivity of Orf2-catalyzed aromatic prenylations Biochemistry
16539380 2006-03-23 Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides Journal of medicinal chemistry
15959519 2005-06-16 Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products Nature
11677123 2001-11-19 Synthesis and photophysical properties of new fluorinated benzo[c]xanthene dyes as intracellular pH indicators Bioorganic & medicinal chemistry letters
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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