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708-76-9 | 2-Hydroxy-4,6-dimethoxybenzaldehyde
CAS No: 708-76-9 Catalog No: AG003KJO MDL No:MFCD00003328
Product Description
Catalog Number:
AG003KJO
Chemical Name:
2-Hydroxy-4,6-dimethoxybenzaldehyde
CAS Number:
708-76-9
Molecular Formula:
C9H10O4
Molecular Weight:
182.1733
MDL Number:
MFCD00003328
IUPAC Name:
2-hydroxy-4,6-dimethoxybenzaldehyde
InChI:
InChI=1S/C9H10O4/c1-12-6-3-8(11)7(5-10)9(4-6)13-2/h3-5,11H,1-2H3
InChI Key:
FQRQWPNYJOFDLO-UHFFFAOYSA-N
SMILES:
COc1cc(OC)cc(c1C=O)O
EC Number:
211-904-1
Properties
Complexity:
171
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
182.058g/mol
Formal Charge:
0
Heavy Atom Count:
13
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
182.175g/mol
Monoisotopic Mass:
182.058g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
55.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5
Literature
| Title | Journal |
|---|---|
| {3,3',5,5'-Tetra-meth-oxy-2,2'-[ethane-1,2-diylbis(nitrilo-methyl-idyne)]diphenolato}nickel(II). | Acta crystallographica. Section E, Structure reports online 20100601 |
| {3,3',5,5'-Tetra-meth-oxy-2,2'-[ethane-1,2-diylbis(nitrilo-methyl-idyne)]diphenol-ato}-copper(II). | Acta crystallographica. Section E, Structure reports online 20100601 |
| 2-[(2,4-Dimethyl-phen-yl)imino-meth-yl]-3,5-dimethoxy-phenol. | Acta crystallographica. Section E, Structure reports online 20090701 |
| 3,5-Dimeth-oxy-2-[(4-propyl-phen-yl)imino-meth-yl]phenol. | Acta crystallographica. Section E, Structure reports online 20090401 |
| 2-[(4-Bromo-phen-yl)imino-meth-yl]-3,5-dimethoxy-phenol. | Acta crystallographica. Section E, Structure reports online 20090401 |
| Antimicrobial properties of substituted salicylaldehydes and related compounds. | Zeitschrift fur Naturforschung. C, Journal of biosciences 20070101 |
| Investigations of intramolecular hydrogen bonding in three types of Schiff bases by 2H and 3H NMR isotope effects. | Magnetic resonance in chemistry : MRC 20040601 |
| The ortho backbone amide linker (o-BAL) is an easily prepared and highly acid-labile handle for solid-phase synthesis. | Journal of combinatorial chemistry 20020101 |
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