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Sigma-Aldrich

Methyl 3-iodo-4-methoxybenzoate

98%

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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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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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

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