2-Amino-5-Chlorbenzaldehyd, 97 %, Thermo Scientific Chemicals
2-Amino-5-Chlorbenzaldehyd, 97 %, Thermo Scientific Chemicals
2-Amino-5-Chlorbenzaldehyd, 97 %, Thermo Scientific Chemicals
2-Amino-5-Chlorbenzaldehyd, 97 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Amino-5-Chlorbenzaldehyd, 97 %, Thermo Scientific Chemicals

CAS: 20028-53-9 | C7H6ClNO | 155.581 g/mol
Have Questions?
Ansicht ändernbuttonViewtableView
Menge:
1 g
5 g
Katalognummer L17515.03
auch als L17515-03 bezeichnet
Preis (EUR)
63,30
Each
Zum Warenkorb hinzufügen
Menge:
1 g
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
63,30
Each
Zum Warenkorb hinzufügen
Chemikalien-Kennzeichnungen
CAS20028-53-9
IUPAC Name2-amino-5-chlorobenzaldehyde
Molecular FormulaC7H6ClNO
InChI KeyKUIFMGITZFDQMP-UHFFFAOYSA-N
SMILESNC1=C(C=O)C=C(Cl)C=C1
Mehr anzeigen
SpecificationsSpecification SheetDatenblatt
Appearance (Color)Dark yellow to yellow to orange to brown
FormCrystals or powder or crystalline powder or fused solid or granules
Assay (HPLC)≥96.0%
Free acid (titration)≤1.5%
Melting Point (clear melt)67.0-76.0?C
2-Amino-5-Chlorobenzaldehyde is used as a raw material in organic synthesis. It also serves as a pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Anwendungen
2-Amino-5-chlorbenzaldehyd wird als Rohstoff in der organischen Synthese verwendet. Es dient auch als pharmazeutisches Zwischenprodukt.

Löslichkeit
Schwer in Wasser löslich.

Hinweise
Luftempfindlich. Nicht kompatibel mit starken Oxidationsmitteln.
RUO – Research Use Only

Allgemeine Referenzen:

  1. Smuszkiewicz, A.; López-Sanz, J.; Pérez-Mayoral, E.; Soriano, E.; Sobczak, I.; Ziolek, M.; Martín-Aranda, R. M.; López-Peinado, A. J. Amino-grafted mesoporous materials based on MCF structure involved in the quinoline synthesis. Mechanistic insights. J. Mol. Catal. A: Chem. 2013, 378, 38-46.
  2. Smuszkiewicz, A.; Pérez-Mayoral, E.; Soriano, E.; Sobczak, I.; Ziolek, M.; Martín-Aranda, R. M.; López-Peinado, A. J. Bifunctional mesoporous MCF materials as catalysts in the Friedländer condensation. Catal. Today 2013, 218-219, 70-75.
  3. Nammalwar, B.; Murie, M.; Fortenberry, C.; Bunce, R. A. Quinoline- and 1,8-naphthyridine-3-carboxylic acids using a self-catalyzed Friedländer approach. Tetrahedron Lett. 2014, 55 (20), 3181-3183.
  4. Gouda, M. A.; Sabah, M. A.; Aljuhani, W. K.; El-Gahani, A. S.; El-Enazi, S. A. E.; Al Enizi, S. A.; Al-Balawi, M. M. Utility of 2-cyano-N-(2-hydroxyethyl) acetamide in heterocyclic synthesis. Eur. J. Chem.2015, 6 (2), 219-224.