Skip to Content
MilliporeSigma
All Photos(1)

Documents

532568

Sigma-Aldrich

Methyl 3-iodo-4-methoxybenzoate

98%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3OC6H3(I)CO2CH3
CAS Number:
35387-93-0
Molecular Weight:
292.07
MDL number:
MFCD00052925
UNSPSC Code:
12352100
PubChem Substance ID:
24877895
NACRES:
NA.22

assay

98%

mp

92-95 °C (lit.)

SMILES string

COC(=O)c1ccc(OC)c(I)c1

InChI

1S/C9H9IO3/c1-12-8-4-3-6(5-7(8)10)9(11)13-2/h3-5H,1-2H3

InChI key

GHNGBFHLUOJHKP-UHFFFAOYSA-N

Application

Methyl 3-iodo-4-methoxybenzoate (1,3-Dimethyl-1H-pyrazol-5-amine) may be used in the preparation of:
  • methyl 3-[3-(N,N-dimethylamino)prop-1-ynyl]-4-methoxybenzoate
  • 3,4,5,2′-tetramethoxybiphenyl
  • 5-propyl-3-ol-1,3-dimethyl-1H-pyrazolo[3,4-b]pyridine

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Aucuparin and Methoxyaucuparin, Two Phenolic Biphenyl.
Erdtman H, et al.
Acta Chemica Scandinavica, 17(4), 1151-1156 (1963)
M Lamothe et al.
Journal of medicinal chemistry, 40(22), 3542-3550 (1997-11-14)
The synthesis and binding affinity at cloned h5-HT1D, h5-HT1D, and h5-HT1A receptors of 3-[3-(N,N-dimethylamino)propyl]-4-hydroxy- N-[4-(pyridin-4-yl)phenyl]benzamide (2, GR-55562) and four O-methylated analogs are described. The functional activity of these compounds was determined at the h5-HT1B receptor using a [35S]GTP gamma S
Sandip B Bharate et al.
Bioorganic & medicinal chemistry, 16(15), 7167-7176 (2008-07-16)
In the present article, we have synthesized three different series of pyrazolo[3,4-b]pyridines and their structural analogues using novel synthetic strategy involving one-pot condensation of 5,6-dihydro-4H-pyran-3-carbaldehyde/2-formyl-3,4,6-tri-O-methyl-D-glucal/chromone-3-carbaldehyde with heteroaromatic amines. All synthesized compounds were evaluated for their anti-inflammatory activity against TNF-alpha and

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