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Key Documents

515183

Sigma-Aldrich

Methyl 4-amino-3-iodobenzoate

95% (GC)

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About This Item

Linear Formula:
H2NC6H3(I)CO2CH3
CAS Number:
Molecular Weight:
277.06
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95% (GC)

mp

86-91 °C (lit.)

SMILES string

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

InChI

1S/C8H8INO2/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4H,10H2,1H3

InChI key

MRLVFVTVXSKAMX-UHFFFAOYSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

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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Pyrrolidinobenzoic acid inhibitors of influenza virus neuraminidase: The hydrophobic side chain influences type A subtype selectivity.
Li Y, et al.
Bioorganic & Medicinal Chemistry, 20(14), 4582-4589 (2012)
Targeting aldehyde dehydrogenase: a potential approach for cell labeling.
Vaidyanathan G, et al.
Nuclear Medicine and Biology, 36(8), 919-929 (2009)
Solid-phase synthesis of an AB loop mimetic of the Ce3 domain of human IgE: Macrocyclization by Sonogashira coupling.
Spivey AC, et al.
The Journal of Organic Chemistry, 68(5), 1843-1851 (2003)
C-N bond formation via Cu-catalyzed cross-coupling with boronic acids leading to methyl carbazole-3-carboxylate: synthesis of carbazole alkaloids.
Rasheed SK, et al.
Royal Society of Chemistry Advances, 4(10), 4960-4969 (2014)

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