Home Other Building Blocks 2,6-Dihydroxynaphthalene

2,6-Dihydroxynaphthalene

CAS No.:
581-43-1
Catalog Number:
AG0035C7
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$18
- +
5g
95%
In Stock USA
United States
$53
- +
10g
95%
In Stock USA
United States
$79
- +
25g
95%
In Stock USA
United States
$143
- +
100g
95%
In Stock USA
United States
$475
- +
Product Description
Catalog Number:
AG0035C7
Chemical Name:
2,6-Dihydroxynaphthalene
CAS Number:
581-43-1
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
MDL Number:
MFCD00004082
IUPAC Name:
naphthalene-2,6-diol
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
SMILES:
Oc1ccc2c(c1)ccc(c2)O
EC Number:
209-465-6
UNII:
4XX2ND0257
NSC Number:
62687
Properties
Complexity:
140  
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:
2.3  
Literature
Title Journal
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
Properties