31172-77-7

Basic information

• Product Name: N,N'-bis<(S)-(1-phenylethyl)>thiourea
• Synonyms: N,N'-bis<(S)-(1-phenylethyl)>thiourea
• CAS NO: 31172-77-7
• Molecular Weight: 284.425
• Mol File: 31172-77-7.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: N,N'-bis<(S)-(1-phenylethyl)>thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-bis<(S)-(1-phenylethyl)>thiourea(31172-77-7)
• EPA Substance Registry System: N,N'-bis<(S)-(1-phenylethyl)>thiourea(31172-77-7)

Safety Data

• Hazardous Substances Data: 31172-77-7(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 24277-43-8 (S)-1-phenylethyl isothiocyanate 
• 24277-44-9 (1-isothiocyanato-ethyl)-benzene 
• 618-36-0 rac-methylbenzylamine 
• 100-42-5 styrene 
• 463-71-8 thiophosgene 
• 105519-65-1 (S)-N-(1-phenylethyl)ammonium (S)-N-(1-phenylethyl)dithiocarbamate 

Relevant articles and documents

Solvent-free synthesis of chiral N,N′-disubstituted thioureas by 'just mixing' the reagents

The synthesis of new chiral thioureas 3a-f by using the ecofriendly solvent-free and microwave-assisted approaches is reported and, unexpectedly, in the former method by just mixing the starting materials the products are instantaneously obtained. The crystal structures for 3b, 3c and 3e are also reported.

Structurally simple chiral thioureas as chiral solvating agents in the enantiodiscrimination of α-hydroxy and α-amino carboxylic acids

C2-Symmetrical chiral thioureas (S,S)-1 and (S,S)-2 were prepared in good yield by the reaction of 2 equiv of inexpensive (S)-1-phenylethylamine, or the corresponding naphthyl analog, with 1 equiv of thiophosgene in the presence of excess triet

Thioureas and their cyclized derivatives: Synthesis, conformational analysis and antimicrobial evaluation

Several single enantiomer thioureas have been synthesized and have been converted to their cyclic derivatives: 2-imino-thiazolidin-4-ones. The conformations of the thioureas have been determined in solution and in the solid state. In solution; an intercon

Recognition of chiral carboxylates by 1,3-disubstituted thioureas with 1-arylethyl scaffolds

Chiral thioureas with 1-arylethyl and 1-arylethyl-2-2-2-trifluoroethyl (Ar = Ph, 1-Napht, 9-Anthr) scaffolds were used as hosts to recognize acetate and chiral mandelates. The higher binding obtained with the trifluoromethyl analogue is also reflected in