98027-84-0
98027-84-0
Chemical Structure
2,6-Dichloro-4-iodopyridine
- CAS No.: 98027-84-0
- Formula:C5H2Cl2IN
- Molecular Weight:273.89
IUPAC Name: 2,6-dichloro-4-iodopyridine
InChIKey: NGSKFMPSBUAUNE-UHFFFAOYSA-N
SMILES: ClC1=CC(I)=CC(Cl)=N1
Biological Activity: 2,6-Dichloro-4-iodopyridine is a biochemical reagent. 2,6-Dichloro-4-iodopyridine is commonly used as a highly reactive synthetic building block and versatile intermediate in organic synthesis, medicinal chemistry, and proteomics research[1][2][3][4].
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2,6-Dichloro-4-iodopyridine | 99.10% | 2,6-Dichloro-4-iodopyridine is a biochemical reagent. 2,6-Dichloro-4-iodopyridine is commonly used as a highly reactive synthetic building block and versatile intermediate in organic synthesis, medicinal chemistry, and proteomics research. | ||||||||||||||||||||
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References
- [1]. Mello JV, et al. Convenient synthesis and transformation of 2,6-dichloro-4-iodopyridine. Organic letters. 2001 Dec 27;3(26):4263-5.
- [2]. Craig RA 2nd, et al. Discovery of Potent and Selective Dual Leucine Zipper Kinase/Leucine Zipper-Bearing Kinase Inhibitors with Neuroprotective Properties in In Vitro and In Vivo Models of Amyotrophic Lateral Sclerosis. J Med Chem. 2022;65(24):16290-16312.
- [3]. Christiansen E, et al. Identification of a Potent and Selective Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist with Favorable Physicochemical and in Vitro ADME Properties. J Med Chem. 2011;54(19):6691-6703.
- [4]. Van de Poël A, et al. Structure-Based Exploration of Selectivity for ATM Inhibitors in Huntington's Disease. J Med Chem. 2021;64(8):5018-5036.
