1572036-99-7

Basic information

• Product Name: C₁₈H₁₉N₅S
• Synonyms: C₁₈H₁₉N₅S
• CAS NO: 1572036-99-7
• Molecular Weight: 337.448
• Mol File: 1572036-99-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₈H₁₉N₅S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₁₉N₅S(1572036-99-7)
• EPA Substance Registry System: C₁₈H₁₉N₅S(1572036-99-7)

Safety Data

• Hazardous Substances Data: 1572036-99-7(Hazardous Substances Data)

Upstream product

• 1942-52-5 2-(diethylamino)ethanethiol hydrochloride 
• 72111-65-0 5-chloro-6-phenylpyrazine-2,3-dicarbonitrile 

Downstream Products

• 927874-90-6 octa(tert-butylsulfanyl)tetrapyrazinoporphyrazinato magnesium(II) 
• 1572038-54-0 C₆₀H₇₃MgN₁₇S₇ 

Relevant articles and documents

Structural factors influencing the intramolecular charge transfer and photoinduced electron transfer in tetrapyrazinoporphyrazines

A series of unsymmetrical tetrapyrazinoporphyrazines (TPyzPzs) from the group of azaphthalocyanines with one peripherally attached amino substituent (donor) were synthesized, and their photophysical properties (fluorescence quantum yield and singlet oxygen quantum yield) were determined. The synthesized TPyzPzs were expected to undergo intramolecular charge transfer (ICT) as the main pathway for deactivating their excited states. Several structural factors were found to play a critical role in ICT efficiency. The substituent in the ortho position to the donor center significantly influences the ICT, with tert-butylsulfanyl and butoxy substituents inducing the strongest ICTs, whereas chloro, methyl, phenyl, and hydrogen substituents in this position reduce the efficiency. The strength of the donor positively influences the ICT efficiency and correlates well with the oxidation potential of the amines used as the substituents on the TPyzPz as follows: n-butylamine a photoinduced electron transfer in which the donor and the acceptor are connected through an aliphatic linker.