2,6-Dihydroxynaphthalene

Product Information

Molecular Formula:
C10H8O2
Molecular Weight:
160.17
Description
2,6-Dihydroxynaphthalene can produce convulsions in mice. Monooxylosylated 2,6-Dihydroxynaphthalene exhibits antiproliferative activity towards certain cells.
Synonyms
naphthalene-2,6-diol
IUPAC Name
naphthalene-2,6-diol
Canonical SMILES
C1=CC2=C(C=CC(=C2)O)C=C1O
InChI
InChI=1S/C10H8O2/c11-9-3-1-7-5-10(12)4-2-8(7)6-9/h1-6,11-12H
InChI Key
MNZMMCVIXORAQL-UHFFFAOYSA-N
Boiling Point
246.06 °C (rough estimate)
Melting Point
223-225 °C
Purity
98 %
Density
1.33 g/cm3
Appearance
Plates or crystals
Storage
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers.
Refractive Index
1.5418 (estimate)
LogP
2.25100
Vapor Pressure
0.00000715 [mmHg]

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
2.3
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
140
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
CN-114134590-A High-performance liquid crystal polyarylester fiber and preparation method and production equipment thereof 2021-12-30
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
JP-2022022261-A Resin composition 2021-11-22
JP-2022027768-A Resin composition 2021-11-16
CN-113845775-A Preparation method of hyperbranched polymer modified boron nitride heat-conducting and insulating composite material 2021-11-08
CN-113929846-A High-carbon-formation-rate water-soluble phenolic resin and preparation method thereof 2021-10-22
JP-2022017350-A Adhesive sheet with support 2021-10-19
CN-113637153-A Multi-block polyether type high-molecular surfactant and preparation method and application thereof 2021-10-18

Literatures

PMID Publication Date Title Journal
20140918 2010-03-15 A light-controlled molecular brake with complete ON-OFF rotation Chemistry (Weinheim an der Bergstrasse, Germany)
20099891 2010-02-19 Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives The Journal of organic chemistry
20689716 2010-01-01 New thermal and microbial resistant metal-containing epoxy polymers Bioinorganic chemistry and applications
19615911 2009-08-15 Chromane derivatives of small aromatic molecules: Chemoenzymatic synthesis and growth inhibitory activity on human tumor cell line LoVo WT Bioorganic & medicinal chemistry
19055354 2009-01-16 Experimental and theoretical studies on constitutional isomers of 2,6-dihydroxynaphthalene carbaldehydes. Effects of resonance-assisted hydrogen bonding on the electronic absorption spectra The Journal of organic chemistry
21202680 2008-05-30 4,4'-(2,6-Dihydroxy-naphthalene-1,5-diyldimethyl-ene)dipyridinium bis-(per-chlorate) Acta crystallographica. Section E, Structure reports online
17479998 2007-06-04 Toward high-generation rotaxane dendrimers that incorporate a ring component on every branch: noncovalent synthesis of a dendritic [10]pseudorotaxane with 13 molecular components Chemistry, an Asian journal
16539380 2006-03-23 Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides Journal of medicinal chemistry
15809167 2005-05-02 The influence of aromatic residues in hydraphile spacer units: assay by ion selective electrode methods and in bacteria Bioorganic & medicinal chemistry
15807536 2005-04-12 Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase Biochemistry
The molarity calculator equation

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

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

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