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86-65-7 | 7-Aminonaphthalene-1,3-disulfonic acid
CAS No: 86-65-7 Catalog No: AG004KXH MDL No:MFCD00003991
Product Description
Catalog Number:
AG004KXH
Chemical Name:
7-Aminonaphthalene-1,3-disulfonic acid
CAS Number:
86-65-7
Molecular Formula:
C10H9NO6S2
Molecular Weight:
303.3116
MDL Number:
MFCD00003991
IUPAC Name:
7-aminonaphthalene-1,3-disulfonic acid
InChI:
InChI=1S/C10H9NO6S2/c11-7-2-1-6-3-8(18(12,13)14)5-10(9(6)4-7)19(15,16)17/h1-5H,11H2,(H,12,13,14)(H,15,16,17)
InChI Key:
CMOLPZZVECHXKN-UHFFFAOYSA-N
SMILES:
Nc1ccc2c(c1)c(cc(c2)S(=O)(=O)O)S(=O)(=O)O
EC Number:
201-689-2
UNII:
7C482FX29K
NSC Number:
4013
Properties
Complexity:
531
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
302.987g/mol
Formal Charge:
0
Heavy Atom Count:
19
Hydrogen Bond Acceptor Count:
7
Hydrogen Bond Donor Count:
3
Isotope Atom Count:
0
Molecular Weight:
303.303g/mol
Monoisotopic Mass:
302.987g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
152A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0
Literature
| Title | Journal |
|---|---|
| One-pot labeling-based capillary zone electrophoresis for separation of amino acid mixture and assay of biofluids. | Analytica chimica acta 20111010 |
| Sandstones of unexpectedly high diffusibility. | Journal of contaminant hydrology 20110325 |
| Induced intersystem crossing at the fluorescence quenching of laser dye 7-amino-1,3-naphthalenedisulfonic acid by paramagnetic metal ions. | Journal of fluorescence 20100101 |
| Antiangiogenic activity of 2-deoxy-D-glucose. | PloS one 20100101 |
| Ultraviolet photodissociation at 355 nm of fluorescently labeled oligosaccharides. | Analytical chemistry 20080701 |
| Fluorophore-assisted carbohydrate electrophoresis: a sensitive and accurate method for the direct analysis of dolichol pyrophosphate-linked oligosaccharides in cell cultures and tissues. | Methods (San Diego, Calif.) 20050401 |
| A novel water-soluble fluorescent probe for the determination of methylamine. | Fresenius' journal of analytical chemistry 20011001 |
| Electrophoretic sequencing of heparin/heparan sulfate oligosaccharides using a highly sensitive fluorescent end label. | Proteomics 20010201 |
| Structure-activity relationship studies with symmetric naphthalenesulfonic acid derivatives. Synthesis and influence of spacer and naphthalenesulfonic acid moiety on anti-HIV-1 activity. | Journal of medicinal chemistry 19930709 |
| Potential anti-AIDS naphthalenesulfonic acid derivatives. Synthesis and inhibition of HIV-1 induced cytopathogenesis and HIV-1 and HIV-2 reverse transcriptase activities. | Journal of medicinal chemistry 19921225 |
| Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses. | Journal of medicinal chemistry 19710701 |
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