257966
2,5-Dimethoxybenzoic acid
98%
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About This Item
Linear Formula:
(CH3O)2C6H3CO2H
CAS Number:
Molecular Weight:
182.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-503-0
MDL number:
Product Name
2,5-Dimethoxybenzoic acid, 98%
InChI key
NYJBTJMNTNCTCP-UHFFFAOYSA-N
InChI
1S/C9H10O4/c1-12-6-3-4-8(13-2)7(5-6)9(10)11/h3-5H,1-2H3,(H,10,11)
SMILES string
COc1ccc(OC)c(c1)C(O)=O
assay
98%
mp
76-78 °C (lit.)
Application
2,5-Dimethoxybenzoic acid has been used in synthesis of:
- galbulimima alkaloid GB 13
- 3,4-dihydrofluoren-2(1H)-ones via reductive alkylation
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Lewis N Mander et al.
Journal of the American Chemical Society, 125(9), 2400-2401 (2003-02-27)
This contribution describes a synthetic approach to alkaloid GB 13, previously isolated from the North Australian and Papua New Guinean rain forest tree Galbulimima belgraveana. A Birch reductive alkylation of 2,5-dimethoxybenzoic acid by 3-methoxybenzyl bromide, followed by an acid-catalyzed cyclization
Reductive alkylation of 2, 5-dimethoxybenzoic acid: a direct synthesis of dihydrofluoren-2-ones.
Hook JM and Mander LN.
The Journal of Organic Chemistry, 45(9), 1722-1724 (1980)
Erick F de Oliveira et al.
Journal of photochemistry and photobiology. B, Biology, 214, 112081-112081 (2020-11-27)
The objective of this study was to investigate synergistic antibacterial activity based on a combination of UV-A light and three classes of food grade compounds: benzoic acid derivatives, cinnamic acid derivatives, and gallates. By using Escherichia coli O157:H7 as the
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