4251-16-5

Usage

Uses

Used in Flavoring Industry:
Propyl thiocyanate is used as a flavoring agent for enhancing the taste of various food products, capitalizing on its naturally pungent aroma derived from its presence in certain foods.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, propyl thiocyanate serves as a key compound in the production of medications, leveraging its chemical properties for the development of new drugs.
Used in Antioxidant Applications:
Propyl thiocyanate is studied for its potential antioxidant properties, which could contribute to health and wellness by combating oxidative stress and related conditions.
Used in Anticancer Research:
Propyl thiocyanate is also under investigation for its possible anticancer effects, suggesting that it might play a role in cancer prevention or treatment strategies in the future.

InChI:InChI=1/C4H7NS/c1-2-3-6-4-5/h2-3H2,1H3

Upstream product

• 506-68-3 bromocyane 
• 4110-50-3 ethyl propyl sulfide 
• 540-54-5 1-Chloropropane 
• 333-20-0 potassium thioacyanate 
• 84703-64-0 phosphoric acid-chloride dimethylamide-propyl ester 
• 106-94-5 propyl bromide 
• 69626-76-2 2-propoxy-4,5-benzo-1,3,2-dioxaphospholane 
• 592-87-0 lead(II) thiocyanate 
• 107-08-4 1-iodo-propane 

Downstream Products

• 76936-70-4 thiophosphoric acid O,O'-dimethyl ester S-propyl ester 
• 20195-06-6 O,O-diethyl-S-n-propyl phosporothiolate 
• 10147-36-1 n-propanesulfonyl chloride 
• 13889-92-4 n-propyl chlorothioformate 
• 69674-00-6 diisopropoxythiophosphoryl isothiocyanate 
• 3253-29-0 O,O,O,O-tetraisopropyl pyrophosphorotrithioate 
• 763-98-4 S-propyl dithiocarbamate 
• 75-08-1 ethanethiol 
• 61680-00-0 O,O-dipropyl phosphoroisothiocyanatidothioate 
• 61614-88-8 bis(O,O'-di-propylphosphorothioyl) sulfide 
• 150-60-7 dibenzyl disulphide 
• 629-19-6 Dipropyl disulfide 
• 4328-22-7 O,O,O,O-tetraethyl trithiopyrophosphate 
• 26190-34-1 O,O-diethyl thiophosphoric acid isothiocyanate 

Relevant academic research and scientific papers

A new synthesis of alkane and polyfluoroalkanesulfonyl chlorides

This study describes a new and advantageous procedure for the synthesis of alkanesulfonyl chlorides (2) by the reaction of alkyl thiocyanates (1) with sulfuryl chloride in a mixture of acetic acid and water. The alkanesulfonyl chlorides were obtained in good yields.

2-Hydroxy-N,N,N-tributylethanaminium thiocyanate as solvent and reagent for the preparation of alkyl thiocyanates

2-Hydroxy-N,N,N-tributylethanaminium thiocyanate was utilized as both solvent and reagent for the conversion of alkyl halides to the corresponding alkyl thiocyanates in good yields under mild conditions.

SYNTHESIS OF ISOTHIOCYANATOPHOSPHORANES AND ISOTHIOCYANATOPHOSPHONIUM SALTS VIA OXIDATIVE ADDITION OF THIOCYANOGEN AND LIGAND SUBSTITUTION. NOVEL REAGENTS FOR CONVERTING HYDROXY GROUPS INTO THIOCYANATE AND ISOTHIOCYANATE FUNCTIONS UNDER MILD CONDITIONS

The oxidative addition of thiocyanogen to triphenilphosphine has been investigated by (31)P NMR spectroscopy showing the formation of the isothiocyanatophosphonium salt 8.The analogous reaction between thiocyanogen and alkyl o-phenylene phosphites 7 leads to diisothiocyanatophosphoranes 9.The same products were prepared via ligand substitution from the corresponding chlorophosphonium salt 12 and alkyldichloro-o-phenylene phosphoranes 13 by the action of potassium thiocyanate in the presence of 18-crown-6-ether or more conveniently using lead thiocyanate.The phosphonium salt 8 and phosphoranes 9 were employed as convenient novel reagents for converting hydroxy groups into thiocyanate and isothiocyanate function with high stereoselectivity under very mild conditions.The efficient synthesis of acylisothiocyanates RCONCS,R2P(O)NCS and R2P(S)NCS via addition of thiocyanogen to mixed anhydrides is of special interest.