1401113-30-1

Basic information

• Product Name: C₂₆H₂₃N₃O₂S
• Synonyms: C₂₆H₂₃N₃O₂S
• CAS NO: 1401113-30-1
• Molecular Weight: 441.554
• Mol File: 1401113-30-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₆H₂₃N₃O₂S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₆H₂₃N₃O₂S(1401113-30-1)
• EPA Substance Registry System: C₂₆H₂₃N₃O₂S(1401113-30-1)

Safety Data

• Hazardous Substances Data: 1401113-30-1(Hazardous Substances Data)

Upstream product

• 616-13-7 1-chloro-2-methylbutane 
• 92-84-2 10H-phenothiazine 
• 1401113-26-5 C₁₈H₁₉NOS 
• 555-21-5 4-Nitrophenylacetonitrile 
• 68825-35-4 C₁₇H₁₉NS 

Relevant articles and documents

Synthesis of organic phenothiazine-based molecular glasses and effect of racemic/homochiral aliphatic chain on near-infrared photorefractive property

Organic near-infrared photorefractive molecular glasses with a phenothiazine moiety are designed and synthesized through the introduction of linear, racemic/homochiral asymmetrically branched aliphatic chains into photorefractive chromophore as an auxiliary group. The compounds are characterized with 1H-NMR, IR, FAB-MS, UV-vis, TG, DSC, etc. The effect of different aliphatic chains on the absorption and thermal properties is investigated in detail. The molar absorption coefficiency at the absorption maximum wavelength showed that the homochiral asymmetrically branched aliphatic chain has a strong hypochromic effect in the dilute solution when it is introduced into photorefractive chromophore. The DSC measurement indicated that the introduction of asymmetrically branched aliphatic chain is the key issue to design organic molecular glasses whether it is racemic or homochiral. The effect of racemic/homochiral asymmetrically branched aliphatic groups on photorefractive property is investigated carefully with poly(N-vinylcarbazole) (PVK) as a photoconductor and with (2,4,7-trinitro-9-fluorenylidene) malononitrile (TNFM) as a photosensitizer. The results suggested that the racemic group is more beneficial to the improvement of photorefractive performance than the homochiral when the homochiral cannot induce rigid photorefractive chromophore to be much more ordered.