1415263-09-0

Basic information

• Product Name: C₃₂H₃₅N₇O₉
• Synonyms: C₃₂H₃₅N₇O₉
• CAS NO: 1415263-09-0
• Molecular Weight: 661.671
• Mol File: 1415263-09-0.mol

Chemical Properties

• CAS DataBase Reference: C₃₂H₃₅N₇O₉(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₂H₃₅N₇O₉(1415263-09-0)
• EPA Substance Registry System: C₃₂H₃₅N₇O₉(1415263-09-0)

Safety Data

• Hazardous Substances Data: 1415263-09-0(Hazardous Substances Data)

Upstream product

• 1415263-04-5 C₂₅H₄₁N₅O₆ 
• 1415262-97-3 C₁₉H₁₈N₂O₉ 
• 601-89-8 2-nitroresorcinol 
• 3163-15-3 2-aminoresorcinol 
• 499-83-2 Pyridine-2,6-dicarboxylic acid 
• 3739-94-4 2,6-Pyridinedicarbonyl dichloride 
• 1415262-96-2 N-(2,6-Dihydroxyphenyl)-4-nitrobenzamide 
• 122-04-3 4-nitro-benzoyl chloride 

Relevant articles and documents

Stabilization of near identical hydrogen bonded octameric water clusters in crystal structures of three distinct non-charged polyamide macrocyclic host molecules

In this paper, we present a comparative analysis of the solid state structures of three wellresolved hydrates of macrocyclic host molecules 1a, 1b, and 2 containing an intrannular amide-aryl substituent (lariat arm) connected to a fixed 26-membered ring in a normal (-NHCOAr, hosts 1a and 1b) or reverse manner (-CONHAr, host 2). Despite different chemical structures, these hosts crystallize as isostructural tetrahydrates in the same P-1 space group. Moreover, their crystals exhibit identical hydrogen bond motifs resulting in a stabilization of an almost identical unusual octameric water cluster built from the cyclic tetramer core and four water molecules, attached sequentially in an “up-and-down” manner. Further analysis reveals that, among the series, the structure of host 2 provides the most suitable environment for the accommodation of this type of water cluster.

A General Method for Synthesis of Unclosed Cryptands via H-Bond Templated Macrocyclization and Subsequent Mild Postfunctionalization

A practical four-step synthesis of a model 26-membered N-Boc-protected macrocycle, starting from commercially available and inexpensive materials, is reported. The crucial macrocyclization step does not require high-dilution conditions and is completed in

"Unclosed cryptands": A point of departure for developing potent neutral anion receptors

Six macrocyclic lariat-type compounds, representing a new class of anion receptors, were synthesized in a simple approach. We identified the optimal macroring size and the position of the hydrogen bond donating center in the lariat arm offering the best a