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Merck
CN

381071

2-Aminoterephthalic acid

99%

Synonym(s):

2-Aminobenzene-1,4-dicarboxylic acid

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About This Item

Linear Formula:
H2NC6H3-1,4-(CO2H)2
CAS Number:
10312-55-7
Molecular Weight:
181.15
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
24863787
MDL number:
MFCD00134536
Beilstein/REAXYS Number:
2805625

Key Documents

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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)

SMILES string

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

InChI key

GPNNOCMCNFXRAO-UHFFFAOYSA-N

assay

99%

form

powder, crystals or chunks

reaction suitability

reaction type: solution phase peptide synthesis

mp

324 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

100

Related Categories

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF7778V
MKCZ6788
MKCZ3449
MKCZ3448
WXBF5906V

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An amino-modified Zr-terephthalate metal?organic framework as an acid?base catalyst for cross-aldol condensation
Vermoortele F, et al.
Chemical Communications (Cambridge, England), 47(5), 1521-1523 (2011)
Weiwei Zhao et al.
PloS one, 12(6), e0178513-e0178513 (2017-06-06)
UiO-66 analogues are good candidates as stationary phase in HPLC because of their chemical/thermal stability, large surface area, and two cage structures. Here, two UiO-66 analogues, UiO-66-NH2 and UiO-67, were synthesized and used as stationary phase in HPLC to evaluate
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
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
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
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