Furan-2-ylmethanethiol

Names
Preferred IUPAC name (Furan-2-yl)methanethiol
Other names Furan-2-ylmethanethiol (2-Furanyl)methylmercaptan 2-Furfurylmercaptan Furfuryl mercaptan 2-Furfurylthiol Furfuryl thiol 2-Furylmethanethiol 2-Furylmethyl mercaptan 2-(Mercaptomethyl)furan
Identifiers
CAS Number	98-02-2 Y
3D model (JSmol)	Interactive image Interactive image
Beilstein Reference	383594
ChemSpider	7085 Y
ECHA InfoCard	100.002.390
EC Number	202-628-2
MeSH	furfuryl+mercaptan
PubChem CID	7363
RTECS number	LU2100000
UNII	29W096TCPG Y
UN number	3336
CompTox Dashboard (EPA)	DTXSID7052654
InChI InChI=1S/C5H6OS/c7-4-5-2-1-3-6-5/h1-3,7H,4H2 Y Key: ZFFTZDQKIXPDAF-UHFFFAOYSA-N Y
SMILES SCc1ccco1 SCC1=CC=CO1
Properties
Chemical formula	C5H6OS
Molar mass	114.16 g·mol−1
Appearance	Colourless liquid
Odor	Roasted coffee, Caramel, Sulfurous, Waxy
Density	1.132 g cm−3
Boiling point	155 °C; 311 °F; 428 K
Vapor pressure	531 Pa
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H226
Flash point	45 °C (113 °F; 318 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose)	100-200 mg kg−1 (mouse)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is YN ?) Infobox references

Furan-2-ylmethanethiol (2-Furanmethanethiol) is an organic compound containing a furan substituted with a sulfanylmethyl group. It is a clear colourless liquid when pure, but it becomes yellow coloured upon prolonged standing. It possesses a strong odour of roasted coffee and a bitter taste. It is a key component of the aroma of roasted coffee. It has been identified as a trigger molecule for parosmia following COVID-19 infection.^[1][2]

Synthesis

Furan-2-ylmethanethiol is easily prepared by reacting furfuryl alcohol with thiourea in hydrochloric acid via an intermediate isothiouronium salt which is hydrolized to the thiol by heating with sodium hydroxide.^[3]

References

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