Misplaced Pages

2-Chloroethyl ethyl sulfide

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
2-Chloroethyl ethyl sulfide
Names
Preferred IUPAC name 1-Chloro-2-(ethylsulfanyl)ethane
Other names 1-Chloro-2-(ethylthio)ethane, 2-(Ethylthio)chloroethane 2-Chlorodiethyl sulfide
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.010.676 Edit this at Wikidata
EC Number
  • 211-742-1
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C4H9ClS/c1-2-6-4-3-5/h2-4H2,1H3Key: GBNVXYXIRHSYEG-UHFFFAOYSA-N
SMILES
  • CCSCCCl
Properties
Chemical formula C4H9ClS
Molar mass 124.63 g·mol
Appearance colorless liquid
Density 1.0663 g/cm
Boiling point 156 °C (313 °F; 429 K)
Hazards
GHS labelling:
Pictograms GHS02: FlammableGHS05: CorrosiveGHS06: ToxicGHS07: Exclamation markGHS08: Health hazard
Signal word Danger
Hazard statements H226, H301, H302, H311, H314, H331, H350
Precautionary statements P201, P202, P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P281, P301+P310, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P310, P311, P312, P321, P322, P330, P361, P363, P370+P378, P403+P233, P403+P235, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

2-Chloroethyl ethyl sulfide is the organosulfur compound with the formula C2H5SC2H4Cl. It is a colorless liquid. The compound is part of the family of vesicant compounds known as half mustards, has been heavily investigated because of its structural similarity to the sulfur mustard S(C2H4Cl)2. The LD50s of the half and full mustard are 252 and 2.4 mg/kg (oral, rats).

References

  1. Wang, Qi-Qiang; Begum, Rowshan Ara; Day, Victor W.; Bowman-James, Kristin (2012). "Sulfur, Oxygen, and Nitrogen Mustards: Stability and Reactivity". Organic & Biomolecular Chemistry. 10 (44): 8786–8793. doi:10.1039/c2ob26482j. PMID 23070251.
Blood agents
Blister agents
Arsenicals
  • Ethyldichloroarsine (ED)
  • Methyldichloroarsine (MD)
  • Phenyldichloroarsine (PD)
  • Lewisite (L)
  • Lewisite 2 (L2)
  • Lewisite 3 (L3)
  • Sulfur mustards
    Nitrogen mustards
    Nettle agents
    Other
    Nerve agents
    G-agents
    V-agents
    GV agents
    Novichok agents
    Carbamates
    Other
    Precursors
    Neurotoxins
    Pulmonary/
    choking agents
    Vomiting agents
    Incapacitating
    agents
    Lachrymatory
    agents
    Malodorant agents
    Cornea-clouding agents
    Biological toxins
    Other
    Sulfur mustards
    Vesicants
    Antineoplastic agents
    • S-46
    • S-112
    • S-150
    • S-163
    • S-169
    • S-170
    • S-172
    • S-173
    • S-179
    • S-180
    • S-182
    • TL-1002
    Other


    Stub icon

    This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

    Categories: