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381071

Sigma-Aldrich

2-Aminoterephthalic acid

99%

Sinónimos:

2-Aminobenzene-1,4-dicarboxylic acid

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About This Item

Fórmula lineal:
H2NC6H3-1,4-(CO2H)2
Número de CAS:
10312-55-7
Peso molecular:
181.15
Beilstein/REAXYS Number:
2805625
MDL number:
MFCD00134536
UNSPSC Code:
12352106
PubChem Substance ID:
24863787
NACRES:
NA.22

assay

99%

form

powder, crystals or chunks

reaction suitability

reaction type: solution phase peptide synthesis

mp

324 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cc(ccc1C(O)=O)C(O)=O

InChI

1S/C8H7NO4/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3H,9H2,(H,10,11)(H,12,13)

InChI key

GPNNOCMCNFXRAO-UHFFFAOYSA-N

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Application

2-Aminoterephthalic acid can be used to synthesize:
  • Lanthanide coordination polymers with 1,10-phenanthroline by hydrothermal method.
  • Blue-emitting derivatives of 2-aminoterephthalic acid.
  • Amino-functionalized Zr-terephthalate (UiO-66), an excellent catalyst for selective synthesis of jasminaldehyde.
  • IRMOF-3, a zinc aminoterephthalate metal-organic framework useful as a catalyst for the Knoevenagel condensation of benzaldehyde and ethyl cyanoacetate.
  • Polymeric composite membrane with excellent CO2 separation capabilities.

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Yuqian Jia et al.
Journal of chromatography. A, 1551, 21-28 (2018-04-14)
A core-shell discoid shaped indium (III) sulfide@metal-organic framework (MIL-125(Ti)) nanocomposite was synthesized by a solvothermal method and explored as an adsorbent material for dispersive solid-phase extraction (d-SPE). The as-synthesized sorbent was characterized by scanning electron microscopy, energy-dispersive spectroscopy, transmission electron
Zhiyong Tang et al.
Biosensors & bioelectronics, 101, 253-259 (2017-11-03)
We are presenting an electrochemical immunosensor for the determination of Galectin-3 (Gal-3), a biomarker of heart failure. A glassy carbon electrode (GCE) was modified with a film of a composite made from the N-doped graphene nanoribbons immobilized Fe-based-Metal-organic frameworks deposited
Supramolecular architecture of new lanthanide coordination polymers of 2-aminoterephthalic acid and 1, 10-phenanthroline
Liu CB, et al.
New. J. Chem., 28(8), 1019-1026 (2004)
On the photostability of some blue-emitting derivatives of 2-aminoterephthalic acid and their copolymers with methyl methacrylate
Miladinova P, et al.
Polymer Degradation and Stability, 98(11), 2347-2350 (2013)
Dangchen Ma et al.
ACS applied materials & interfaces, 11(48), 45290-45300 (2019-11-14)
For the first time, continuous polycrystalline UiO-66-NH2 thin film supported by a cross-linked Matrimid substrate was successfully fabricated via in situ solvothermal synthesis at room temperature for organic solvent nanofiltration. The integrated structure of the formed UiO-66-NH2 selective layer was
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