Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

159603

Sigma-Aldrich

Methyl 3,5-dihydroxybenzoate

97%

Sign Into View Organizational & Contract Pricing

Select a Size

25 G
$59.60
100 G
$221.00

$59.60

In StockDetails

Request a Bulk Order
All Photos(1)

Select a Size

Change View
25 G
$59.60
100 G
$221.00

About This Item

Linear Formula:
(HO)2C6H3CO2CH3
CAS Number:
2150-44-9
Molecular Weight:
168.15
EC Number:
218-426-2
MDL number:
MFCD00002289
UNSPSC Code:
12352100
PubChem Substance ID:
24849826
NACRES:
NA.22
form:
solid
assay:
97%

$59.60

In StockDetails

Request a Bulk Order

Quality Level

100

assay

97%

form

solid

mp

167-170 °C (lit.)

functional group

ester

SMILES string

COC(=O)c1cc(O)cc(O)c1

InChI

1S/C8H8O4/c1-12-8(11)5-2-6(9)4-7(10)3-5/h2-4,9-10H,1H3

Inchi Key

RNVFYQUEEMZKLR-UHFFFAOYSA-N

Related Categories

General description

Ribonucleotide reductase inhibiton and antiumor activity of methyl 3,5-dihydroxybenzoate has been studied.[1]

Application

Methyl 3,5-dihydroxybenzoate was used in the synthesis of cored dendrimers.[2] 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.[3]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBB3148V
STBB3148
04204TE
03904ME
S38186

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service