159603
Methyl 3,5-dihydroxybenzoate
97%
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About This Item
Linear Formula:
(HO)2C6H3CO2CH3
CAS Number:
Molecular Weight:
168.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-426-2
MDL number:
Product Name
Methyl 3,5-dihydroxybenzoate, 97%
form
solid
InChI key
RNVFYQUEEMZKLR-UHFFFAOYSA-N
InChI
1S/C8H8O4/c1-12-8(11)5-2-6(9)4-7(10)3-5/h2-4,9-10H,1H3
SMILES string
COC(=O)c1cc(O)cc(O)c1
assay
97%
mp
167-170 °C (lit.)
functional group
ester
Quality Level
Related Categories
Application
Methyl 3,5-dihydroxybenzoate was used in the synthesis of cored dendrimers. It was also used in the preparation of bis(5-carbomethoxy-1,3-phenylene)-32-crown-10, a semi-rigid 32-membered ring diester crown ether.
General description
Ribonucleotide reductase inhibiton and antiumor activity of methyl 3,5-dihydroxybenzoate has been studied.
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
Regulatory Information
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New ribonucleotide reductase inhibitors with antineoplastic activity.
H L Elford et al.
Cancer research, 39(3), 844-851 (1979-03-01)
Synthesis of cored dendrimers.
Wendland MS and Zimmerman SC.
Journal of the American Chemical Society, 121(6), 1389-1390 (1999)
Macrocyclic polymers. 1. Synthesis of a poly (ester crown) based on bis (5-carboxy-1, 3-phenylene)-32-crown-10 and 4, 4'-isopropylidenediphenol (bisphenol A).
Delaviz Y and Gibson HW.
Macromolecules, 25(1), 18-20 (1992)
Shota Machida et al.
Molecules (Basel, Switzerland), 24(23) (2019-12-01)
Twenty-one natural and unnatural phenolic compounds containing a carbohydrate moiety were synthesized and their structure-activity relationship (SAR) was evaluated for α-glucosidase inhibition and antioxidative activity. Varying the position of the galloyl unit on the 1,5-anhydro-d-glucitol (1,5-AG) core resulted in changes
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