68860-35-5

Basic information

• Product Name: Phosphonium, [(3-formyl-4-hydroxyphenyl)methyl]triphenyl-, chloride
• CAS NO: 68860-35-5
• Molecular Formula: C26H22O2P.Cl
• Molecular Weight: 432.886
• Mol File: 68860-35-5.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Phosphonium, [(3-formyl-4-hydroxyphenyl)methyl]triphenyl-, chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium, [(3-formyl-4-hydroxyphenyl)methyl]triphenyl-, chloride(68860-35-5)
• EPA Substance Registry System: Phosphonium, [(3-formyl-4-hydroxyphenyl)methyl]triphenyl-, chloride(68860-35-5)

Safety Data

• Hazardous Substances Data: 68860-35-5(Hazardous Substances Data)

Upstream product

• 90-02-8 salicylaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 
• 23731-06-8 5-(chloromethyl)salicylaldehyde 
• 603-35-0 triphenylphosphine 

Downstream Products

• 68860-34-4 2-hydroxy-5-vinylbenzaldehyde 

Relevant articles and documents

Zinc (II) complex with a cationic Schiff base ligand: Synthesis, characterization, and biological studies

A cationic Schiff base ligand, TSB (L) and its Zn (II) complex (1) were synthesized and characterized by using CHN, 1H-NMR, FT-IR, UV, LC-MS, and X-ray methods. Their ability to inhibit topoisomerase I, DNA cleavage activities, and cytotoxicity

Benzimidazole derivative and 8-hydroxyquinoline derivative cadmium complex dye sensitizer as well as preparation method and application thereof

The invention relates to a D (-A-pi-A) 2 type benzimidazole derivative and 8-hydroxyquinoline derivative cadmium complex dye sensitizer (BDTT-bi-Cd) as shown in a formula 1 as well as a preparation method and application of the BDTT-bi-Cd. The dye sensitizer is a D (-A-pi-A) 2 type complex synthesized by reacting benzimidazole containing functional groups such as an auxiliary electron acceptor (A), a pi bridge, a main electron acceptor (A) and an anchoring group with a 8-hydroxyquinoline derivative cadmium complex and an electron donor (D) benzodithiophene bithiophene (BDTT) through a Heck coupling reaction. Experiments show that the photovoltaic performance test of a dye-sensitized solar cell with the BDTT-bi-Cd as the dye sensitizer shows good effects that the photoelectric conversion efficiency (PCE) reaches 8.40%, the dye thermal decomposition temperature reaches 320 DEG C or above, the thermal stability is high, the requirements of photovoltaic materials can be met, and the complex dye sensitizer has a certain prospect in the aspect of development and application of the dye-sensitized solar cell. The structure of the complex BDTT-bi-Cd shown in the formula 1 is shown in the specification.

Sterol regulatory element binding protein and acidic nucleoplasm DNA binding protein-1 inhibitor, preparation method and application thereof

The invention discloses a compound which is shown as formula I and can inhibit sterol regulatory element binding protein (Srebp) and acidic nucleoplasm DNA binding protein-1 (And-1, WDHD1), a preparation method and application thereof. RT-PCR (reverse transcription-polymerase chain reaction) and immunoblotting experiments show that the compound can remarkably reduce the expression of a Srebp downstream gene SCD-1 and inhibit the activity of And-1 protein. Further experiments show that the compound has a proliferation inhibition effect on various tumor cells. The compound shown as formula I isexpected to become a novel anti-tumor drug and a tumor chemoradiotherapy sensitizing drug.