2371-06-4 Usage
Explanation
The compound consists of 8 carbon atoms, 17 hydrogen atoms, and 1 chlorine atom.
Explanation
1-Chloro-2,2,4-trimethylpentane is a modified version of isooctane, with a chlorine atom added to the structure.
Explanation
Isooctane, the non-chlorinated version of 1-chloro-2,2,4-trimethylpentane, is commonly used as a reference point for measuring the octane rating of gasoline.
Explanation
The chlorine atom in 1-chloro-2,2,4-trimethylpentane makes it a valuable reagent in the synthesis of other organic compounds.
Explanation
1-Chloro-2,2,4-trimethylpentane is employed as a solvent in various chemical processes and as an intermediate in the production of other chemicals.
Explanation
The chemical is prone to catching fire and can ignite under certain conditions.
Explanation
Exposure to 1-chloro-2,2,4-trimethylpentane can cause discomfort and irritation in the respiratory system, on the skin, and in the eyes.
Chlorinated derivative
2,2,4-trimethylpentane (isooctane)
Gasoline octane rating reference
isooctane
Organic synthesis utility
Chlorine atom presence
Uses
Solvent and chemical production intermediate
Flammability
Flammable
Health hazards
Respiratory irritation, skin irritation, eye irritation
Check Digit Verification of cas no
The CAS Registry Mumber 2371-06-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2371-06:
(6*2)+(5*3)+(4*7)+(3*1)+(2*0)+(1*6)=64
64 % 10 = 4
So 2371-06-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H17Cl/c1-7(2)5-8(3,4)6-9/h7H,5-6H2,1-4H3
2371-06-4Relevant articles and documents
Tabushi et al.
, p. 81 (1973)
MECHANISMS OF FREE-RADICAL REACTIONS. XV. SELECTIVITY OF THE FREE-RADICAL CHLORINATION OF ALIPHATIC HYDROCARBONS BY ARYLCHLOROIODONIUM CHLORIDES
Dneprovskii, A. S.,Krainyuchenko, I. V.,Kasatochkin, A. N.
, p. 437 - 440 (2007/10/02)
The free-radical chlorination of 2,3-dimethylbutane, 2,2,4-trimethylpentane, adamantane, and cyclohexane by arylchloroiodonium chlorides was investigated by the method of competing reactions.It was shown that the introduction of electron-withdrawing substituents into the arylchloroiodonium chloride leads to an increase in the sensitivity of the process to the polar effect of the substituents in the substrate and to a decrease of the selectivity toward variation in the dissociation energy of the C - H bond.The importance of steric effects in the reaction was noted.
