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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

Quality Level

100

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
Jianhao Qiu et al.
Chemosphere, 242, 125197-125197 (2019-11-02)
Industrial effluents often contain mixed metal ions and dyes, and it is difficult to efficiently remove both types of contaminants simultaneously. Here, MIL-125-NH2@Ag/AgCl composites were for the first time developed through a facile deposition-photoreduction method for simultaneously removing Cr(VI)/Rhodamine B
Kristian Blindheim Lausund et al.
Dalton transactions (Cambridge, England : 2003), 46(48), 16983-16992 (2017-11-28)
Thin films of metal-organic frameworks (MOFs) prepared using all-gas-phase techniques such as atomic/molecular layer deposition (ALD/MLD) are emerging due to their potential for enabling suitable applications. Their high and specific porosity enables their use as membranes for separations and as
Hsuan-Lan Wang et al.
ACS applied materials & interfaces, 10(11), 9332-9341 (2018-03-02)
We report an aerosol-based approach to study the thermal stability of metal-organic frameworks (MOFs) for gas-phase synthesis of MOF-based hybrid nanostructures used for highly active catalysis. Temperature-programmed electrospray-differential mobility analysis (TP-ES-DMA) provides the characterization of temperature-dependent morphological change directly in
Hao Zhang et al.
Nanomaterials (Basel, Switzerland), 10(9) (2020-09-17)
A combination of calcination and hydrothermal processing was used to prepare a g-C3N4/UiO-66-NH2/CdS photocatalyst, and the degradation of tetracycline (TC) over this material was assessed. The photocatalytic performance of this nanocomposite was approximately 4.4 and 2.3 times those of CdS
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