817-97-0

Usage

InChI:InChI=1/C6H11NOS/c1-3-5-7-6(9)8-4-2/h3H,1,4-5H2,2H3,(H,7,9)

Upstream product

• 64-17-5 ethanol 
• 57-06-7 N-allyl isothiocyanate 
• 140-89-6 potassium ethyl xanthogenate 
• 107-11-9 1-amino-2-propene 
• 141-52-6 sodium ethanolate 

Downstream Products

• 869-97-6 3-Allylcarbaminylthio-propionsaeure 
• 92961-25-6 3-allyl-5-(3-nitro-benzylidene)-thiazolidine-2,4-dione 
• 24289-21-2 (E,Z)-5-Benzylidene-3-allyl-2,4-dioxo-1,3-thiazolidine 
• 92851-69-9 3-allyl-5-(3,4-dimethoxy-benzylidene)-thiazolidine-2,4-dione 

Relevant academic research and scientific papers

Identification of new, odor-active thiocarbamates in cress extracts and structure-activity studies on synthesized homologues

New, odorant nitrogen- and sulfur-containing compounds are identified in cress extracts. Cress belongs to the botanical order Brassicales and produces glucosinolates, which are important precursors of nitrogen- and sulfur-containing compounds. Those compo

Niaziminin, a thiocarbamate from the leaves of Moringa oleifera, holds a strict structural requirement for inhibition of tumor-promoter-induced epstein- barr virus activation

Three known thiocarbamate (TC)- and isothiocyanate (ITC)-related compounds have been isolated from the leaves of Moringa oleifera, a traditional herb in southeast Asia, as inhibitors of tumor promoter teleocidin B-4-induced Epstein- Barr virus (EBV) activ

Process for the preparation of N-allyl-O-alkyl thionocarbamates

An improvement in the process for the preparation of N-allyl-O-alkyl thionocarbamates by the reaction of an allyl isothiocyanate with an alcohol is disclosed which comprises the use of a catalyst of the general formula: STR1 wherein R1, R2, R3, R4, and R5 are individually selected from alkyl or aryl or a mixture thereof, M represents a metal from Group III B, IV B, or V B of the Periodic Table of the Elements, and n is the integer 0 or 1; provided that the sum of n1, n2, n3, n4, and n5 equals the valance of said metal M.