693-07-2 Usage
Description
2-Chloroethyl ethyl sulfide is a monofunctional analog of sulfur mustard (SM; 2,2'-dichloro diethyl sulfide), characterized by its clear colorless to light yellow liquid appearance. It is also recognized as a chemical warfare agent simulant, with its mass diffusivity being a subject of study.
Uses
Used in Research and Development:
2-Chloroethyl ethyl sulfide is utilized as a research compound for the development of countermeasures and protective measures against chemical warfare agents. Its properties and behavior provide valuable insights into the understanding of sulfur mustard and related chemical threats.
Used in Environmental and Safety Studies:
As a simulant for chemical warfare agents, 2-chloroethyl ethyl sulfide is employed in environmental and safety studies to evaluate the effectiveness of decontamination procedures and safety measures in the event of exposure to such agents.
Used in Medical and Pharmaceutical Research:
2-Chloroethyl ethyl sulfide serves as a model compound in medical and pharmaceutical research, aiding in the development of antidotes and treatments for exposure to sulfur mustard and similar chemical agents. Its unique chemical properties contribute to the advancement of medical countermeasures and protective gear.
Safety Profile
Poison by ingestion and
subcutaneous routes. Mutation data
reported. A severe skin and eye irritant. See
also ETHERS and SULFIDES. When heated to decomposition it emits very toxic
fumes of Cland SOx.
Check Digit Verification of cas no
The CAS Registry Mumber 693-07-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 693-07:
(5*6)+(4*9)+(3*3)+(2*0)+(1*7)=82
82 % 10 = 2
So 693-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H9ClS/c1-2-6-4-3-5/h2-4H2,1H3
693-07-2Relevant articles and documents
New preparative procedure for the synthesis of chloroalkyl sulfides
Russavskaya,Korchevin,Alekminskaya,Sukhomazova,Levanova,Deryagina
, p. 1445 - 1448 (2007/10/03)
Reaction of thiols with dihaloalkanes in the system hydrazine hydrate-base leads to alkyl(chloroalkyl) sulfides with different positions of the chlorine atom with respect to sulfur. The developed one-step procedure for the synthesis of such unsymmetrical sulfides is most suitable for arenethiols and alkanethiols having a long polymethylene chain. The reaction mechanism is discussed.
A POLYMERIC ANALOG OF DIMETHYL SULFOXIDE: SYNTHESIS OF CROSSLINKED POLYMERS WITH BOUND SULFOXIDE GROUPS
Janout, Vaclav,Hrudkova, Hana,Cefelin, Pavel
, p. 1563 - 1568 (2007/10/02)
By using a sequence of functionalization reactions, a series of crosslinked polymers with pendant sulfoxide units of the P-(CH2SOCH2)nR type with n=1,2,3 and R= H, CH3, where P is poly(styrene-co-divinylbenzene) (content of the crosslinking component 1percent, 2percent) were prepared.The high reactivity of the crosslinked polymeric thiol P-CH2SH in alkylation reactions was used in the preparation.Conditions for the selective oxidation of polymeric sulfides to sulfoxides were checked.