22007-29-0

Upstream product

• 124-41-4 sodium methylate 
• 2131-61-5 p-nitrophenyl isothiocyanate 
• 67-56-1 methanol 

Downstream Products

• 913341-20-5 (1,1'-bis(diphenylphosphino)ferrocene)digold(I)(SC(OMe)=N(4-nitrophenyl))2 
• 913341-18-1 (1,3-bis(diphenylphosphino)propane)digold(I)(SC(OMe)=N(4-nitrophenyl))2 
• 913341-11-4 (triethylphosphine)gold(I)(SC(OMe)=N(4-nitrophenyl)) 
• 913341-16-9 (bis(diphenylphosphino)methane)digold(I)(SC(OMe)=N(4-nitrophenyl))2 
• 913341-17-0 (1,2-bis(diphenylphosphino)ethane)digold(I)(SC(OMe)=N(4-nitrophenyl))2 
• 913341-19-2 (1,4-bis(diphenylphosphino)butane)digold(I)(SC(OMe)=N(4-nitrophenyl))2 
• 913341-15-8 (triphenylphosphine)gold(I)(SC(OMe)=N(4-nitrophenyl)) 
• 913341-13-6 (tricyclohexylphosphine)gold(I)(SC(OMe)=N(4-nitrophenyl)) 

Relevant academic research and scientific papers

Glycosyl alkoxythioimidates as building blocks for glycosylation: A reactivity study

Structural modifications of the leaving group of S-glycosyl O-methyl phenylcarbamothioates (SNea) involving change of substituents that express different electronic effects led to a better understanding of how the reactivity of these glycosyl donors can b

The Kinetics and Mechanism of Addition of Water and Alcohols to p-Nitrophenyl Isothiocyanate. The Effects of Added Dimethyl Sulphoxide

The second order-rate constants for the addition of water and ethanol to p-nitrophenyl isothiocyanate are larger in dimethyl sulphoxide solution than in pure water or ethanol.The detailed behaviour over a wide composition range suggests that H-bonding by