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Merck
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Key Documents

381071

Sigma-Aldrich

2-Aminoterephthalic acid

99%

동의어(들):

2-Aminobenzene-1,4-dicarboxylic acid

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About This Item

Linear Formula:
H2NC6H3-1,4-(CO2H)2
CAS Number:
Molecular Weight:
181.15
Beilstein:
2805625
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

99%

형태

powder, crystals or chunks

반응 적합성

reaction type: solution phase peptide synthesis

mp

324 °C (dec.) (lit.)

응용 분야

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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애플리케이션

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.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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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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