63918-89-8 Usage
Description
BIS(2-(2-CHLOROETHYLTHIO)ETHYL)ETHER is a colorless liquid that solidifies at 10°C (50°F) and has a boiling point of 120°C (248°F). It has a density of 1.24 at 25°C (77°F) and readily dissolves in common organic solvents, while being slightly soluble in water.
Uses
Used in Chemical Industry:
BIS(2-(2-CHLOROETHYLTHIO)ETHYL)ETHER is used as a chemical intermediate for the synthesis of various compounds due to its reactive nature and ability to dissolve in common organic solvents.
Used in Pharmaceutical Industry:
BIS(2-(2-CHLOROETHYLTHIO)ETHYL)ETHER is used as a reagent in the production of pharmaceuticals, taking advantage of its solubility properties and chemical reactivity.
Used in Research and Development:
BIS(2-(2-CHLOROETHYLTHIO)ETHYL)ETHER is utilized in research and development settings for studying its chemical properties and potential applications in various fields, including material science and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 63918-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,1 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63918-89:
(7*6)+(6*3)+(5*9)+(4*1)+(3*8)+(2*8)+(1*9)=158
158 % 10 = 8
So 63918-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16Cl2OS2/c9-1-5-12-7-3-11-4-8-13-6-2-10/h1-8H2
63918-89-8Relevant articles and documents
Unexpected Reaction Pathways Leading to Thiodiglycol during the Degradation of Long-Chain Sulfur Mustards
Gómez-Caballero, Esther,Martínez-álvarez, Roberto,Sierra, Miguel A.
, p. 12432 - 12439 (2018/10/15)
Degradation of long-chain sulfur mustards with various commercial decontaminants unexpectedly forms thiodiglycol (TDG) through unreported reaction pathways. Chemical warfare agents (CWAs) degradation products have to be unambiguously related to their reference compounds in order to fulfill international verification protocols. Thus, the formation of TDG using water-based decontaminants introduces an uncertainty in the origin of this chemical that has been systematically used to unambiguously demonstrate the presence of yperite in environmental and biomedical samples. Therefore, these novel and unprecedented degradation pathways will result either in modifications of the international verification protocols for forensic purposes or in the exclusion of TDG as an exclusive marker of yperite.
