1395348-29-4

Basic information

• Product Name: C₃₀H₂₁N₃O₃
• Synonyms: C₃₀H₂₁N₃O₃
• CAS NO: 1395348-29-4
• Molecular Weight: 471.515
• Mol File: 1395348-29-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: C₃₀H₂₁N₃O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₂₁N₃O₃(1395348-29-4)
• EPA Substance Registry System: C₃₀H₂₁N₃O₃(1395348-29-4)

Safety Data

• Hazardous Substances Data: 1395348-29-4(Hazardous Substances Data)

Upstream product

• 33143-80-5 3-(p-cyanophenoxy)-1-propyne 
• 7753-13-1 4,4′,4″-(1,3,5-triazine-2,4,6-triyl)triphenol 
• 106-96-7 propargyl bromide 

Relevant articles and documents

Triazine-cored dendritic molecules containing multiple o-carborane clusters

A series of C3-symmetricaltriazine-cored small dendritic molecules containing three to nine peripheral o-carborane clusters were synthesized through Cu(I)-catalyzedazide–alkyne cycloaddition reactions. The newly synthesized molecules containing multiple o-carborane moieties were characterized using nuclear magnetic resonance and matrix-assisted laser desorption/ionization-time of flight mass spectral analysis. The biological evaluation of these three to nine cage dendrimers was performed using breast cancer cells (Michigan Cancer Foundation 7). All these dendritic compounds showed cytotoxicity toward breast cancer cells, and the toxicity increased as the number of peripheral o-carboranes increased. The 9-cage molecule showed the highest cytotoxicity, and the half maximal inhibitory concentration (IC50) value was found to be 80.67 ng/ml. Its cytotoxicity was significantly higher than the common chemotherapy agent cisplatin. As expected, the boron-richo-carborane-appended molecules showed high thermal stability. The thermal stability increased as the number of peripheral o-carborane moieties increased.

Interaction of carborane-appended trimer with bovine serum albumin: A spectroscopic investigation

The interaction of symmetrical triazine-cored carborane-appended trimer 5 with bovine serum albumin has been investigated using different spectroscopic methods. The intrinsic fluorescence of BSA was quenched by the carborane trimer 5 through the dynamic q

Synthesis and structural analysis of some podands with C 3 symmetry

The multistep syntheses of C3-symmetrical tripodands with terminal triple bonds or azide groups exhibiting 1,3,5-triarylbenzene and 2,4,6-triaryl-1,3,5-triazine cores are reported herein. The structures of the newly synthesized compounds are su