Search

  • Order Status
  • Quick Order
  • Promos
Element SearchElement SearchStructure SearchStructure Search
2,3-Dimethoxycinnamic acid, predominantly trans, 98+%
2,3-Dimethoxycinnamic acid, predominantly trans, 98+%
2,3-Dimethoxycinnamic acid, predominantly trans, 98+%
Thermo Scientific Chemicals

2,3-Dimethoxycinnamic acid, predominantly trans, 98+%

CAS: 7345-82-6 | C11H12O4 | 208.213 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
10 g
50 g
250 g
ChemDexTry the chem dexTM web app
Catalog number A15936.30
also known as A15936-30
Price (EUR)
548,00
Each
Quantity:
250 g
Request bulk or custom format
Price (EUR)
548,00
Each
Chemical Identifiers
CAS7345-82-6
IUPAC Name3-(2,3-dimethoxyphenyl)prop-2-enoic acid
Molecular FormulaC11H12O4
InChI KeyQAXPUWGAGVERSJ-UHFFFAOYSA-N
SMILESCOC1=CC=CC(C=CC(O)=O)=C1OC
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Assay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
FormCrystals or powder or crystalline powder
Assay (HPLC)≥98.0%
Melting Point (clear melt)177.0-184.0?C
2,3-Dimethoxycinnamic acid is used in the synthesis of (2E,2E,2E)-N,N,N-(nitrilotri-2,1-ethanediyl)tris[3-(2,3-dimethoxyphenyl)-2-propenamide].

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2,3-Dimethoxycinnamic acid is used in the synthesis of (2E,2′E,2′′E)-N,N′,N′′-(nitrilotri-2,1-ethanediyl)tris[3-(2,3-dimethoxyphenyl)-2-propenamide].

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Nobuko Mibu.; Kazumi Yokomizo.; Wataru Uchida.; Satoshi Takemura.; Jianrong Zhou.; Hatsumi Aki.; Takeshi Miyata.; Kunihiro Sumoto. Molecular symmetry and biological activities of new symmetrical tris(2-aminoethyl)amine derivatives. Chemical & Pharmaceutical Bulletin. 2012, 60 (3), 408-414.
  2. G. Pandey.; A. Krishna. Synthetic application of photoinduced single electron transfer reactions: a convenient synthetic approach for the 2,2-dimethyl-2H-chromene system. J. Org. Chem. 1988, 53 (10), 2364-2365.