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Merck
CN

T22403

Tetrahydrothiophene 1-oxide

96%

Synonym(s):

Tetramethylene sulfoxide

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About This Item

Empirical Formula (Hill Notation):
C4H8OS
CAS Number:
Molecular Weight:
104.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-493-2
Beilstein/REAXYS Number:
105274
MDL number:
Assay:
96%
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Quality Level

assay

96%

refractive index

n20/D 1.52 (lit.)

bp

235-237 °C (lit.)

density

1.158 g/mL at 25 °C (lit.)

SMILES string

O=S1CCCC1

InChI

1S/C4H8OS/c5-6-3-1-2-4-6/h1-4H2

InChI key

ISXOBTBCNRIIQO-UHFFFAOYSA-N



Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

233.6 °F - closed cup

flash_point_c

112 °C - closed cup

ppe

Eyeshields, Gloves



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R Meganathan et al.
Journal of bacteriology, 169(6), 2862-2865 (1987-06-01)
Escherichia coli used tetrahydrothiophene 1-oxide (THTO) as an electron acceptor for anaerobic growth with glycerol as a carbon source; the THTO was reduced to tetrahydrothiophene. Cell extracts also reduced THTO to tetrahydrothiophene in the presence of a variety of electron
Sangeun Yun et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 21(3), 204-211 (2019-12-06)
Lead halide perovskite is one of the attractive functional materials owing to its outstanding opto-electronic properties, which have been addressed in numerous studies. This study aims to clarify the link between the growth pattern and the charge carrier related properties
V K Chadha et al.
Journal of medicinal chemistry, 26(6), 916-922 (1983-06-01)
Sulfoxides and amides were tested as inhibitors of liver alcohol dehydrogenase and ethanol metabolism in rats. With both series of compounds, increasing the hydrophobicity resulted in better inhibition, and introduction of polar groups reduced inhibition. Of the cyclic sulfoxides, tetramethylene



Global Trade Item Number

SKUGTIN
T22403-25G04061837341847