581-43-1 | 2,6-Dihydroxynaphthalene

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$13.00	$9.00
5g	98%	in stock	$25.00	$17.00
25g	98%	in stock	$79.00	$55.00

Description

• Catalog Number: AB46687
• 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

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

Literature

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

  Chemistry (Weinheim an der Bergstrasse, Germany) 20100315

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

  The Journal of organic chemistry 20100219

• New thermal and microbial resistant metal-containing epoxy polymers.

  Bioinorganic chemistry and applications 20100101

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

  Bioorganic & medicinal chemistry 20090815

• 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 20090116

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

  Acta crystallographica. Section E, Structure reports online 20080601

• 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 20070604

• Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides.

  Journal of medicinal chemistry 20060323

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

  Bioorganic & medicinal chemistry 20050502

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

  Biochemistry 20050412

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

  Biotechnology and bioengineering 20050405

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

  Biosensors & bioelectronics 20030501

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

  Chemical communications (Cambridge, England) 20020121

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

  Inorganic chemistry 20010115