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17823-69-7

17823-69-7 Structure

17823-69-7 Structure
IdentificationBack Directory
[Name]

3,3-Bis(methylthio)-2-cyanopropenamide
[CAS]

17823-69-7
[Synonyms]

3-Bis(methylthio)-2-cyanopropenamide
2-Cyano-3,3-bis(methylthio)acrylamide
3,3-Bis(methylthio)-2-cyanopropenamide
2-cyano-3,3-bis(methylthio)-2-Propenamide
2-Propenamide, 2-cyano-3,3-bis(methylthio)-
2-cyano-3,3-bis(methylsulfanyl)prop-2-enamide
[Molecular Formula]

C6H8N2OS2
[MDL Number]

MFCD00205587
[MOL File]

17823-69-7.mol
[Molecular Weight]

188.27
Chemical PropertiesBack Directory
[Melting point ]

101-102 °C
[Boiling point ]

349.7±42.0 °C(Predicted)
[density ]

1.317±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

11.74±0.50(Predicted)
Safety DataBack Directory
[HS Code ]

2930909899
Hazard InformationBack Directory
[Synthesis]

Carbon disulfide

75-15-0

Dimethyl sulfate

77-78-1

2-Cyanoacetamide

107-91-5

3,3-Bis(methylthio)-2-cyanopropenamide

17823-69-7

Preparation of 2-cyano-3,3-bis(methylthio)acrylamide: A mixture of cyanoacetamide (10 g, 118.9 mmol) and potassium hydroxide (6.661 g, 118.9 mmol) in acetonitrile (100 mL) was stirred for 1 hour at room temperature. Subsequently, carbon disulfide (9.054 g, 118.9 mmol) was slowly added at the same temperature and stirring was continued for 3 hours. Next, dimethyl sulfate (19.5 g, 154.6 mmol) was added and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the volatiles were removed under vacuum and the residue was redissolved in ethyl acetate, washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and subsequently concentrated under vacuum. The resulting solid was ground with a solvent mixture of ethyl acetate/hexane, filtered and dried to afford the target compound 2-cyano-3,3-bis(methylthio)acrylamide (9.4 g, 42% yield, 99.0% purity) as a yellow solid.

[References]

[1] Patent: US2016/176857, 2016, A1. Location in patent: Paragraph 0275
[2] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 24, p. 5453 - 5458
[3] Journal of Agricultural and Food Chemistry, 2008, vol. 56, # 13, p. 5242 - 5246
[4] Journal of Heterocyclic Chemistry, 2011, vol. 48, # 4, p. 901 - 906
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