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Thermo Scientific Chemicals
4,6-Dichloropyrimidine-5-carboxaldehyde, 97%
CAS: 5305-40-8 | C5H2Cl2N2O | 176.98 g/mol
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Catalog number H54449.03
also known as H54449-03
Price (USD)
45.80
Each
Quantity:
1 g
Price (USD)
45.80
Each
Chemical Identifiers
CAS5305-40-8
Specifications
Specification Sheet
Specification SheetAppearance (Color)Light yellow
Assay (unspecified)>96.0%
FormCrystalline solid
4,6-Dichloropyrimidine-5-carboxaldehyde is used as a substrate in the synthesis of N-terminal surrogate in amino acid and peptide analogues.
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.
Applications
4,6-Dichloropyrimidine-5-carboxaldehyde is used as a substrate in the synthesis of N-terminal surrogate in amino acid and peptide analogues.
Notes
Incompatible with strong oxidizing agents and strong acids. Store in cool place.
4,6-Dichloropyrimidine-5-carboxaldehyde is used as a substrate in the synthesis of N-terminal surrogate in amino acid and peptide analogues.
Notes
Incompatible with strong oxidizing agents and strong acids. Store in cool place.
RUO – Research Use Only
General References:
- Li, B.; Yue, Z.; Xiang, H.; Lv, L.; Song, S.; Miao, Z.; Yang, C. Catalyst-free synthesis of benzofuran-fused pyrido[4,3-d]pyrimidines from 2-(2-hydroxyaryl)acetonitrile and 4,6-dichloropyrimidine-5-carbaldehyde through domino condensation reactions. RCS Adv. 2015, 4 (1), 358-364.
- Schenone, S.; Radi, M.; Musumeci, F.; Brullo, C.; Botta, M. Biologically Driven Synthesis of Pyrazolo[3,4-d]pyrimidines As Protein Kinase Inhibitors: An Old Scaffold As a New Tool for Medicinal Chemistry and Chemical Biology Studies. Chem. Rev. 2014, 114 (14), 7189-7238.