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393673 Aldrich

1-Methyl-2-aminoterephthalate

98%

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Properties

Related Categories Building Blocks, C8 to C9, Carbonyl Compounds, Chemical Synthesis, Esters,
InChI Key   QKOKLMFCKLEFDV-UHFFFAOYSA-N
assay   98%
mp   217-220 °C(lit.)
solubility   concentrated acid: soluble (HCl)(lit.)

Description

Packaging

5, 25 g in glass bottle

Application

1-Methyl-2-aminoterephthalate is suitable reagent used in the synthesis of 1-methyl-2-iodoterephthalate.

1-Methyl-2-aminoterephthalate may be used in the following syntheses:
• triarylphosphine
• methyl 4-(hydroxymethyl-2-iodobenzoate
• 1-methyl-2-diphenylphosphinoterepthalate

General description

1-Methyl-2-aminoterephthalate (3-Amino-4-carbomethoxybenzoic acid, 3-Amino-4-methoxycarbonylbenzoic acid) is the 1-methyl ester of 2-aminoterephthalic acid.

Price and Availability

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Certificate of Origin

Protocols & Articles

Articles

Nontraceless Staudinger Ligation

Bertozzi et al. pioneered the application of the Staudinger reaction as a ligation method for bioconjugates. In the course of their studies on the metabolic engineering of cell surfaces they designed...
Matthias Junkers
Aldrich ChemFiles 2008, 8.1, 7.
Keywords: Amidations, Catalysis, Chemfiles, Cyclizations, Esterifications, Iodinations, Molecular probes, Peptide synthesis, Staudinger Reaction

Staudinger Ligation - Aldrich ChemFiles 2008, 8.1, 7.

The reaction between an azide and a phosphine forming an aza-ylide was discovered almost a century ago by Nobel Prize laureate Herrmann Staudinger. It has found widespread application in chemical syn...
Matthias Junkers
Aldrich ChemFiles 2008, 8.1, 7.
Keywords: Amidations, Catalysis, Chemfiles, Cyclizations, Eliminations, Esterifications, Glycosylations, Iodinations, Methods, Molecular probes, Peptide synthesis, Reductions, Solid phase peptide synthesis, Staudinger Reaction, Staudinger Reduction, Type, Wittig Reaction

Peer-Reviewed Papers
15

References

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