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About This Item
Empirical Formula (Hill Notation):
C4H8S
CAS Number:
Molecular Weight:
88.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-728-9
Beilstein/REAXYS Number:
102392
MDL number:
Assay:
99%
vapor pressure
18 mmHg ( 25 °C)
Quality Level
assay
99%
refractive index
n20/D 1.504 (lit.)
bp
119 °C (lit.)
mp
−96 °C (lit.)
density
1 g/mL at 25 °C (lit.)
SMILES string
C1CCSC1
InChI
1S/C4H8S/c1-2-4-5-3-1/h1-4H2
InChI key
RAOIDOHSFRTOEL-UHFFFAOYSA-N
Application
Tetrahydrothiophene can be used as a reagent for the synthesis of various epoxides and their derivatives. It can be used as a catalyst for the synthesis of benzo[n.1.0]bicycloalkanes.
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
55.4 °F - closed cup
flash_point_c
13 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Tetrahydrothiophene-catalyzed synthesis of benzo [n.1.0] bicycloalkanes.
Ye LW, et al.
The Journal of Organic Chemistry, 72(4), 1335-1340 (2007)
Catalytic asymmetric synthesis of epoxides from aldehydes using sulfur ylides with in situ generation of diazocompounds.
Aggarwal VK, et al.
Angewandte Chemie (International Edition in English), 40(8), 1430-1433 (2001)
Sanat Ghosh et al.
Physical chemistry chemical physics : PCCP, 22(31), 17482-17493 (2020-06-13)
This is a tale of a pair of a hydrogen bond donor and acceptor, namely the CH donor and sulphur acceptor, neither of which is a conventional hydrogen bond participant. Sulfur (S), being less electronegative (2.58) compared to its first
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T15601-500G | 04061837337857 |
| T15601-5G | 04061837841446 |
| T15601-100G | 04061837337840 |

