1583306-61-9

Basic information

• Product Name: C₃₆H₃₈N₄O₅
• Synonyms: C₃₆H₃₈N₄O₅
• CAS NO: 1583306-61-9
• Molecular Weight: 606.722
• Mol File: 1583306-61-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₃₆H₃₈N₄O₅(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₆H₃₈N₄O₅(1583306-61-9)
• EPA Substance Registry System: C₃₆H₃₈N₄O₅(1583306-61-9)

Safety Data

• Hazardous Substances Data: 1583306-61-9(Hazardous Substances Data)

Upstream product

• 79-08-3 bromoacetic acid 
• 100-46-9 benzylamine 
• 555-96-4 Benzylhydrazine 

Downstream Products

• 1583306-65-3 C₃₆H₃₆N₄O₄ 
• 18084-64-5 N,N’,N’’,N’’’-tetrabenzyl-1,4,7,10-tetraazacyclododecane 

Relevant articles and documents

From Cyclic Peptoids to Peraza-macrocycles: A General Reductive Approach

Peraza-macrocycles form chelates of high thermodynamic and kinetic stability useful in diagnostic imaging (MRI, SPECT, PET), in coordination chemistry, and as catalysts. In this letter, we report an advantageous method to prepare these compounds via BHsu

Solid state assembly of cyclic α-peptoids

The solid state assembly of free and metal coordinated cyclic α-peptoids has been examined with the aim to find common underlying features and to direct the design of new functional biomimetic materials with desired properties in terms of molecular recognition, drug delivery and catalysis. The lack of the amide proton prevents the formation of NH...OC hydrogen bonds and weaker interactions play a key role in the intermolecular recognition and assembly. Inter-annular CH...OC hydrogen bonds provide face to face or side by side arrangement of macrocycles in a way that can be considered the peptoid counterpart of β-sheet secondary structure in proteins. The choice of side chains is crucial for the solid state properties of α-cyclic peptoids. Side chains have a strong influence on the solid state assembly of peptoid macrocycles: they may provide competing interactions to CH...OC inter-annular hydrogen bonds, leading either to a T-shape or to a tubular arrangement of the peptoid macrocycles. The size of the macrocycle is another important factor influencing the tubular arrangement. In particular, a larger size of the macrocycle promotes side by side with respect to T-shape interactions. Hirshfeld surfaces and their fingerprint analysis allowed the analysis of the contributions of weak intermolecular interactions, such as weak CH...OC hydrogen bonds and CH-pi interactions, towards the crystal packing. This journal is the Partner Organisations 2014.