2366-36-1 Usage
Physical state
Colorless, non-flammable, and volatile liquid
Primary use
Refrigerant in air conditioning and cooling systems
Low boiling point
Contributes to its effectiveness as a refrigerant
Thermodynamic properties
Makes it suitable for refrigeration applications
Industrial applications
Used as a solvent in the production of cleaning agents and aerosol propellants
Blowing agent
Used in the production of foam insulation materials
Environmental concerns
Potential for ozone depletion
Regulatory status
Phased out in many countries due to environmental concerns
Alternatives
More environmentally friendly alternatives are being used in place of 1,1,1-trichloro-2-fluoro-ethane
Check Digit Verification of cas no
The CAS Registry Mumber 2366-36-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2366-36:
(6*2)+(5*3)+(4*6)+(3*6)+(2*3)+(1*6)=81
81 % 10 = 1
So 2366-36-1 is a valid CAS Registry Number.
2366-36-1Relevant academic research and scientific papers
REACTIONS OF CHLORINE MONOFLUORIDE. IV. ADDITION OF CHLORINE MONOFLUORIDE TO HALOGEN-SUBSTITUTED ALKENES
Boguslavskaya, L. S.,Chuvatkin, N. N.,Panteleeva, I. Yu.
, p. 1832 - 1842 (2007/10/02)
The reactions of chlorine monofluoride with halogenoethylenes (1,1-dichloro-, 1,2-dichloro-, trichloro-, and tetrachloroethylenes) and halogenopropenes ( 3-bromo-, 3,3,3-trichloro-, E- and Z-1,3-dichloro-, 3-chloro-2-methyl-, and perfluoropropenes) were investigated in inert solvents in the presence of ethyl acetate as external nucleophile.In all cases chloroacyloxy adducts were isolated and identified in addition to the chlorofluorination products, and this indicates an electrophilic mechanism for the chlorofluorination of polyhalogenoalkenes.Methyl chloromaleate, chlorofumarate, chlorofluoroethylenedicarboxylate, α,β-difluoroacrylate, and perfluoromethacrylate in anhydrous hydrogen fluoride form the corresponding chlorofluoro adducts with satisfactory yields, whereas the reaction takes place with difficulty in inert solvents.
