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

Name: 2,3-Dimethoxycinnamic acid, predominantly trans, 98+%
SKU: A15936.30

CAS: 7345-82-6 | C11H12O4 | 208.213 g/mol

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產品號碼 A15936.30

亦稱為 A15936-30

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Quantity:

250 g

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化學識別

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

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規格

規格表

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:

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.
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.