sales@angenesci.com
Login | Register
logo
Structures Search
Home Other Building Blocks 1,6-Dihydroxynaphthalene

1,6-Dihydroxynaphthalene

CAS No.:
575-44-0
Catalog Number:
AG003DR7
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$75
- +
500g
98%(HPLC)
In Stock USA
United States
$287
- +
Product Description
Catalog Number:
AG003DR7
Chemical Name:
1,6-Dihydroxynaphthalene
CAS Number:
575-44-0
Molecular Formula:
C10H8O2
Molecular Weight:
160.1693
MDL Number:
MFCD00003981
IUPAC Name:
naphthalene-1,6-diol
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
SMILES:
Oc1ccc2c(c1)cccc2O
EC Number:
209-386-7
UNII:
34C30KW024
NSC Number:
7201
Properties
Complexity:
158  
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:
1.9  
Literature
Title Journal
[Simultaneous determination of seven naphthalenediols in cosmetics by reversed-phase high performance liquid chromatography]. Se pu = Chinese journal of chromatography 20120601
Various aspects of piscine toxicology. Interdisciplinary toxicology 20100901
Chemoenzymatic syntheses of prenylated aromatic small molecules using Streptomyces prenyltransferases with relaxed substrate specificities. Bioorganic & medicinal chemistry 20080901
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 20070701
Understanding the substrate selectivity and the product regioselectivity of Orf2-catalyzed aromatic prenylations. Biochemistry 20070206
Selective antiproliferative activity of hydroxynaphthyl-beta-D-xylosides. Journal of medicinal chemistry 20060323
Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products. Nature 20050616
Synthesis and photophysical properties of new fluorinated benzo[c]xanthene dyes as intracellular pH indicators. Bioorganic & medicinal chemistry letters 20011119
Properties