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Home Other Building Blocks 3-Methoxyphenylacetic acid

3-Methoxyphenylacetic acid

CAS No.:
1798-09-0
Catalog Number:
AG00279F
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
96%
In Stock USA
United States
$13
- +
25g
96%
In Stock USA
United States
$32
- +
100g
96%
In Stock USA
United States
$113
- +
500g
96%
In Stock USA
United States
$488
- +
Product Description
Catalog Number:
AG00279F
Chemical Name:
3-Methoxyphenylacetic acid
CAS Number:
1798-09-0
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00004334
IUPAC Name:
2-(3-methoxyphenyl)acetic acid
InChI:
InChI=1S/C9H10O3/c1-12-8-4-2-3-7(5-8)6-9(10)11/h2-5H,6H2,1H3,(H,10,11)
InChI Key:
LEGPZHPSIPPYIO-UHFFFAOYSA-N
SMILES:
COc1cccc(c1)CC(=O)O
EC Number:
217-282-8
UNII:
25XLO0T6MY
Properties
Complexity:
156  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
166.063g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
166.176g/mol
Monoisotopic Mass:
166.063g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
46.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
Title Journal
A new facile synthetic route to [11C]GSK189254, a selective PET radioligand for imaging of CNS histamine H3 receptor. Bioorganic & medicinal chemistry letters 20120715
Evaluation of (R)-(-)-α-methoxy phenyl acetic acid as a chiral shift reagent for resolution and determination of R and S enantiomers of modafinil in bulk drugs and formulations by 1H NMR spectroscopy. Chirality 20120401
Anticancer activity of dinuclear gallium(III) carboxylate complexes. European journal of medicinal chemistry 20100201
Study of the cytotoxic activity of di and triphenyltin(IV) carboxylate complexes. Journal of inorganic biochemistry 20081201
Lipophilic (hydroxy)phenylacetates by solvent-free lipase-catalyzed esterification and transesterification in vacuo. Journal of agricultural and food chemistry 20080709
Pilocarpine-induced status epilepticus: monoamine level, muscarinic and dopaminergic receptors alterations in striatum of young rats. Neuroscience letters 20050701
Role of the peri-effect in synthesis and reactivity of highly substituted naphthaldehydes: a novel backbone amide linker for solid-phase synthesis. Organic & biomolecular chemistry 20050207
Contribution of aldehyde oxidase, xanthine oxidase, and aldehyde dehydrogenase on the oxidation of aromatic aldehydes. Chemical research in toxicology 20041001
Properties