93-40-3 | Homoveratric acid

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
25g	98%	in stock	$9.00	$6.00
100g	98%	in stock	$25.00	$17.00
500g	98%	in stock	$66.00	$46.00

Description

• Catalog Number: AB42811
• Chemical Name: Homoveratric acid
• CAS Number: 93-40-3
• Molecular Formula: C10H12O4
• Molecular Weight: 196.1999
• MDL Number: MFCD00004335
• SMILES: COc1cc(ccc1OC)CC(=O)O

Computed Properties

• Complexity: 193
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 1

Upstream Synthesis Route

(3,4-Dimethoxyphenyl) Acetic Acid, also known as DMPA, is a versatile organic compound widely used in chemical synthesis. Its distinct structure, featuring a phenyl ring with two methoxy groups at the 3 and 4 positions, grants it unique properties that make it valuable in various applications. In chemical synthesis, DMPA serves as a crucial building block for developing pharmaceuticals, agrochemicals, and specialty chemicals. Its presence in the molecular structure of the final product can significantly impact its properties, such as stability, solubility, and biological activity. By incorporating (3,4-Dimethoxyphenyl) Acetic Acid into the synthesis process, chemists can tailor the characteristics of the end product to meet specific requirements, paving the way for innovative and impactful advancements in the field of chemistry.

Literature

• Synthesis, biological evaluation and mechanism studies of deoxytylophorinine and its derivatives as potential anticancer agents.

  PloS one 20120101

• Synthesis of homoveratric acid-imprinted polymers and their evaluation as selective separation materials.

  Molecules (Basel, Switzerland) 20110505

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Tetra-kis[μ-2-(3,4-dimeth-oxy-phen-yl)acetato]-κO:O';κO,O':O;κO:O,O'-bis-{[2-(3,4-dimeth-oxy-phen-yl)acetato-κO,O'](1,10-phenanthroline-κN,N')samarium(III)}.

  Acta crystallographica. Section E, Structure reports online 20101101

• Tetra-kis[μ-2-(3,4-dimeth-oxy-phen-yl)acetato]-κO,O:O;κO:O,O;κO:O-bis-{[2-(3,4-dimeth-oxy-phen-yl)acetato-κO,O](1,10-phenanthroline-κN,N')erbium(III)}.

  Acta crystallographica. Section E, Structure reports online 20101101

• Tetra-kis(μ-3,4-dimeth-oxy-phenyl-acetato)-bis-[(3,4-dimeth-oxy-phenyl-acetato)(1,10-phenanthroline)holmium(III)].

  Acta crystallographica. Section E, Structure reports online 20101001

• Alpha-carboxy-6-nitroveratryl: a photolabile protecting group for carboxylic acids.

  The Journal of organic chemistry 20100702

• Racemization-free synthesis of (S)-(+)-tylophorine from L-proline by radical cyclization.

  Organic letters 20100507

• Tetra-kis(μ-3,4-dimethoxy-phenyl-acetato)bis-[(3,4-dimethoxy-phenyl-acetato)(1,10-phenanthroline)dysprosium(III)].

  Acta crystallographica. Section E, Structure reports online 20100301

• Tetra-kis(μ(2)-3,4-dimethoxy-phenyl-acetato)-κO,O':O';κO:O:O';κO:O';κO:O'-bis-[(3,4-dimethoxy-phenyl-acetato-κO,O')(1,10-phenanthroline-κN,N)thulium(III)].

  Acta crystallographica. Section E, Structure reports online 20100101

• Highly efficient formal synthesis of cephalotaxine, using the Stevens rearrangement--acid lactonization sequence as a key transformation.

  The Journal of organic chemistry 20090306

• Synthesis, lipophilicity and antimicrobial activity of new derivatives of thiosemicarbazides and 1,2,4-triazoline-5-thione.

  Acta poloniae pharmaceutica 20090101

• Hydrogen-bonding interactions in (3,4-dimethoxyphenyl)acetic acid monohydrate.

  Acta crystallographica. Section C, Crystal structure communications 20080701

• Reactivity and acid-base behavior of ring-methoxylated arylalkanoic acid radical cations and radical zwitterions in aqueous solution. Influence of structural effects and pH on the benzylic C-H deprotonation pathway.

  The Journal of organic chemistry 20060707

• Contribution of aldehyde oxidizing enzymes on the metabolism of 3,4-dimethoxy-2-phenylethylamine to 3,4-dimethoxyphenylacetic acid by guinea pig liver slices.

  Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 20060101

• Inhibition of brain mitochondrial respiration by dopamine and its metabolites: implications for Parkinson's disease and catecholamine-associated diseases.

  Journal of neurochemistry 20041101

• Enzyme production by Mycena galopus mycelium in artificial media and in Picea sitchensis F1 horizon needle litter.

  Mycological research 20030801