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Merck
CN

292990

S-Furfuryl thioacetate

99%

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About This Item

Empirical Formula (Hill Notation):
C7H8O2S
CAS Number:
Molecular Weight:
156.20
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
237-173-9
MDL number:
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InChI key

LQOUTUIIYXYBQW-UHFFFAOYSA-N

InChI

1S/C7H8O2S/c1-6(8)10-5-7-3-2-4-9-7/h2-4H,5H2,1H3

SMILES string

CC(SCC1=CC=CO1)=O

assay

99%

refractive index

n20/D 1.526 (lit.)

bp

90-92 °C/12 mmHg (lit.)

density

1.171 g/mL at 25 °C (lit.)

Quality Level

Application

S-Furfuryl thioacetate (S-2-furfuryl thioacetate) has been used in lipase (from Candida rugosa) mediated synthesis of 2-furfurylthiol.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

199.4 °F - closed cup

flash_point_c

93 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Rachid Bel Rhlid et al.
Journal of agricultural and food chemistry, 50(14), 4087-4090 (2002-06-27)
Enzymatic hydrolysis of S-3-(2-methylfuryl) thioacetate and S-2-furfuryl thioacetate using lipase from Candida rugosa produced 2-methyl-3-furanthiol and 2-furfurylthiol, respectively. When reactions were carried out at room temperature and pH 5.8, 2-methyl-3-furanthiol was produced in a optimal yield of 88% after 15

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