1048657-24-4

Basic information

• Product Name: C₁₃H₁₈N₂O₃*ClH
• Synonyms: C₁₃H₁₈N₂O₃*ClH
• CAS NO: 1048657-24-4
• Molecular Weight: 286.758
• Mol File: 1048657-24-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₃H₁₈N₂O₃*ClH(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₃H₁₈N₂O₃*ClH(1048657-24-4)
• EPA Substance Registry System: C₁₃H₁₈N₂O₃*ClH(1048657-24-4)

Safety Data

• Hazardous Substances Data: 1048657-24-4(Hazardous Substances Data)

Upstream product

• 1048653-48-0 C₁₁H₁₅NO₂*ClH 
• 888970-78-3 C₂₁H₂₄N₂O₅ 
• 122-00-9 para-methylacetophenone 
• 169032-05-7 (R)-5-methyl-5-(p-tolyl)imidazolidine-2,4-dione 

Downstream Products

• 1048658-26-9 C₂₅H₃₂N₄O₅*ClH 
• 1048657-59-5 C₃₂H₃₆N₄O₇ 
• 888970-76-1 C₅₇H₆₆N₈O₁₁ 
• 1321595-01-0 C₅₆H₆₄N₈O₁₁ 
• 1321595-03-2 C₄₈H₅₈N₈O₉*ClH 
• 888970-74-9 C₄₈H₅₆N₈O₈ 
• 888970-75-0 C₃₃H₃₈N₄O₇ 

Relevant articles and documents

Design and scalable synthesis of new chiral selectors. Part 1: Synthesis and characterization of a new constrained cyclopeptide from unnatural bulky amino acids

We describe the conception, synthesis, and characterization of a novel cyclopeptide designed for chiral recognition. The asymmetric units are built from an unnatural amino acid in the series of α-aryl-α-methyl glycine. Modifications of standard methods of peptide synthesis are described in order to improve yields and purities when applied to hindered amino acids. First set of experiments about host-guest ability of the obtained cyclopeptide is disclosed.