2941-64-2 Usage
Description
Ethyl chlorothioformate, also known as ethyl thionocarbonate, is an amber-colored liquid with a pungent penetrating odor. It is a flammable and toxic chemical compound that is denser than water and has a flash point of 125°F. It is corrosive to metals and tissue, and its vapors are heavier than air.
Uses
Used in Chemical Synthesis:
Ethyl chlorothioformate is used as an intermediate in the chemical synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its reactivity and versatility make it a valuable component in the synthesis of a wide range of products.
Used in Pesticide Production:
Ethyl chlorothioformate is used as a key component in the production of certain pesticides. Its ability to react with other chemicals and form new compounds makes it a useful building block for creating effective and targeted pest control agents.
Used in Rubber Industry:
In the rubber industry, ethyl chlorothioformate is used as a curing agent for certain types of rubber. Its chemical properties allow it to facilitate the cross-linking process, which is essential for the production of durable and high-quality rubber products.
Used in Pharmaceutical Industry:
Ethyl chlorothioformate is used as a reagent in the pharmaceutical industry for the synthesis of various drugs. Its ability to react with other compounds and form new molecules makes it a valuable tool in the development of new medications and therapies.
Used in Research and Development:
Due to its unique chemical properties and reactivity, ethyl chlorothioformate is also used in research and development laboratories. Scientists and researchers utilize this compound to study its properties, explore its potential applications, and develop new methods for its synthesis and use in various industries.
Air & Water Reactions
Flammable. Insoluble in water. On contact with moisture Ethyl chlorothioformate produces highly corrosive and toxic fumes of hydrogen chloride gas.
Reactivity Profile
Special Hazards of Combustion Products: Irritating vapors and toxic gases, such as sulfur oxides, hydrogen chloride, and carbon monoxide, may be formed when involved in fire.
Health Hazard
Exposure can cause irritation of eyes, nose and throat.
Potential Exposure
Used for making other chemicals. A
pharmaceutical intermediate
Shipping
UN2826 Ethyl chlorothioformate, Hazard Class: 8;
Labels: 8-Corrosive material, 6.1-Poison Inhalation Hazard,
3-Flammable liquid; Inhalation Hazard Zone B
Incompatibilities
Corrosive to metals. Flammable vapors
may form explosive mixture with air. Contact with moisture releases highly corrosive and toxic hydrogen chloride
gas. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids,
oxoacids, and epoxides.
Waste Disposal
Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Generators of waste containing this contaminant
(≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal.
Controlled incineration (oxides of nitrogen are removed
from the effluent gas by scrubbers and/or thermal devices)
Check Digit Verification of cas no
The CAS Registry Mumber 2941-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2941-64:
(6*2)+(5*9)+(4*4)+(3*1)+(2*6)+(1*4)=92
92 % 10 = 2
So 2941-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H5ClOS/c1-2-6-3(4)5/h2H2,1H3
2941-64-2Relevant articles and documents
ADENOSINE DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
-
Paragraph 000198, (2021/02/05)
Disclosed here is an adenosine derivative prodrug that can have reverse transcriptase inhibitor activity in vivo. This disclosure is also directed to a pharmaceutical composition comprising the adenosine derivative that can be used for the treatment of HIV infection or RNA virus infection.
Facile 'one-pot' preparation of phosphonothiolformates. Useful reagents for the synthesis of carbamoylphosphonates
Salomon, Claudio J.,Breuer, Eli
, p. 815 - 816 (2007/10/03)
A versatile and mild 'one-pot' reaction for the preparation of trialkyl phosphonothiolformates was accomplished by sequential reaction of phosgene solution with alkanethiols, and subsequent Arbuzov reaction with trialkyl phosphites.
NOVEL SYNTHESIS OF DISUBSTITUTED THIOLCARBAMATES VIA A SULFUR TRANSFER AGENT-POTASSIUM ALKYL OR BENZYL DITHIOCARBONATES
D'Amico, John J.,Schafer, Tann
, p. 301 - 304 (2007/10/02)
The reaction of N,N-disubstituted carbamoyl chlorides with potassium alkyl or benzyl dithiocarbonates afforded a novel synthesis of disubstituted thiolcarbamates.