1000391-87-6

Basic information

• Product Name: 4,6-bis-[2-(4-diethylamino-phenyl)-vinyl]-pyrimidin-2-ol
• Synonyms: 4,6-bis-[2-(4-diethylamino-phenyl)-vinyl]-pyrimidin-2-ol
• CAS NO: 1000391-87-6
• Molecular Weight: 442.604
• Mol File: 1000391-87-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4,6-bis-[2-(4-diethylamino-phenyl)-vinyl]-pyrimidin-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-bis-[2-(4-diethylamino-phenyl)-vinyl]-pyrimidin-2-ol(1000391-87-6)
• EPA Substance Registry System: 4,6-bis-[2-(4-diethylamino-phenyl)-vinyl]-pyrimidin-2-ol(1000391-87-6)

Safety Data

• Hazardous Substances Data: 1000391-87-6(Hazardous Substances Data)

Upstream product

• 34289-60-6 2-oxo-4,6-dimethyl-1,2-dihydropyrimidine hydrochloride 
• 120-21-8 4-Diethylaminobenzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 108-79-2 4,6-dimethyl-2(1H)-pyrimidinone 
• 34289-60-6 4,6-dimethyl-2-hydroxy-pyrimidine hydrochloride 

Downstream Products

• 1036364-92-7 4,6-bis-[2-(4-diethylamino-phenyl)-vinyl]-2-(2-ethyl-hexyloxy)-pyrimidine 
• 1000391-88-7 4,6-bis-[2-(4-diethylaminophenyl)vinyl]-2-chloropyrimidine 
• 1379668-62-8 4-{4,6-bis-[2-(4-(diethylamino)phenyl)vinyl]pyrimidin-2-yloxy}phthalonitrile 
• 1316832-44-6 methyl 4-(4,6-bis(4-(diethylamino)styryl)pyrimidin-2-yloxy)butanoate 
• 1316832-52-6 C₃₅H₄₈N₆O₂ 
• 1316832-50-4 C₄₀H₅₆N₆O₄ 
• 1316832-45-7 4-(4,6-bis(4-(diethylamino)styryl)pyrimidin-2-yloxy)butanoic acid 

Relevant articles and documents

Synthesis, two-photon absorption properties and bioimaging applications of mono-, di- and hexa-branched pyrimidine derivatives

A series of mono-, di- and hexa-branched pyrimidine derivatives possessing two-photon absorption have been synthesized. The spectral features of the dyes showed solvatochromic with significant bathochromic shifting of the emission spectra and large Stokes shifts in more polar solvents mainly due to the intramolecular charge-transfer. The two-photon absorption cross-section values were measured by two-photon excited fluorescence and open aperture Z-scan methods. The results revealed that the two-photon absorption cross-section values were enhanced with increasing electron-donating strength of the end group and branch number. The photophysical properties of the dyes were further investigated with the aid of theoretical calculations. In addition, the di-branched dyes has the largest values of two-photon absorption cross-section per molecular weight, low cytotoxicity and can be internalized by human liver cancer cell line and accumulates in the cytoplasm, allowing for live cell two-photon fluorescence imaging, so it is promising for in vitro and vivo cellular imaging applications.

Synthesis, optical properties and singlet oxygen generation of a phthalocyanine derivative containing strong two-photon-absorbing chromophores in the periphery

A phthalocyanine derivative containing two-photon chromophores which are based on pyrimidine was designed and synthesized. Its light-emission property was studied in detail, and a strong energy transfer from peripheral chromophores to the phthalocyanine c

Two-photon absorption of a series of V-shape molecules: The influence of acceptor's strength on two-photon absorption in a noncentrosymmetric D-π-A-π-D system

A series of V-shape D-π-A-π-D molecules were synthesized based on pyrimidine as the acceptor. The strength of the acceptor (A) in these molecules was systematically adjusted through changing the substituent group in pyrimidine. Their two-photon absorption properties were measured by two-photon induced fluorescence techniques with a mode-locked Ti:sapphire laser (100 fs, 80 MHz) in the range of 720 to 880 nm. The results indicate that the strength of the acceptor has an important influence on the two-photon absorption properties of this noncentrosymmetric D-π-A-π-D system, and a molecule with a strong acceptor is liable to display a large two-photon absorption cross-section. The Royal Society of Chemistry.