817-97-0

Basic information

• Product Name: Allylthiocarbamic acid O-ethyl ester
• Synonyms: Allylthiocarbamic acid O-ethyl ester;N-Allylcarbamothioic acid O-ethyl ester;N-allyl O-ethyl thiocarbamate;N-Allylthiocarbamic acid O-ethyl ester
• CAS NO: 817-97-0
• Molecular Formula: C6H11NOS
• Molecular Weight: 145.2226
• Mol File: 817-97-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 170°Cat760mmHg
• Flash Point: 56.6°C
• Appearance: /
• Density: 1.016g/cm³
• Vapor Pressure: 1.5mmHg at 25°C
• Refractive Index: 1.502
• CAS DataBase Reference: Allylthiocarbamic acid O-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Allylthiocarbamic acid O-ethyl ester(817-97-0)
• EPA Substance Registry System: Allylthiocarbamic acid O-ethyl ester(817-97-0)

Safety Data

• Hazardous Substances Data: 817-97-0(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 29, p. 224, 1964 DOI: 10.1021/jo01024a507

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 
• 141-52-6 sodium ethanolate 
• 140-89-6 potassium ethyl xanthogenate 
• 107-11-9 1-amino-2-propene 

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 articles and documents

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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.