62574-65-6 Usage
Uses
Used in Organic Synthesis:
Pentane, 2-bromo-2,4,4-trimethylis used as a source of the tert-butyl group in organic synthesis for the creation of various organic compounds. Its reactivity allows for the formation of new chemical bonds and the synthesis of complex molecules.
Used in Solvent Applications:
In the chemical industry, Pentane, 2-bromo-2,4,4-trimethylis used as a solvent in organic reactions. Its ability to dissolve a wide range of substances makes it a valuable component in various chemical processes.
Used in Pharmaceutical Production:
Pentane, 2-bromo-2,4,4-trimethylis used as a reagent in the production of pharmaceuticals. Its involvement in the synthesis of drug molecules contributes to the development of new medications and therapies.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, Pentane, 2-bromo-2,4,4-trimethylis utilized in the synthesis of various agrochemicals, such as pesticides and herbicides, to improve agricultural productivity and crop protection.
However, it is crucial to handle Pentane, 2-bromo-2,4,4-trimethylwith caution due to its hazardous nature, potential health risks, and environmental hazards. Proper safety measures and handling protocols should be followed to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 62574-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,7 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62574-65:
(7*6)+(6*2)+(5*5)+(4*7)+(3*4)+(2*6)+(1*5)=136
136 % 10 = 6
So 62574-65-6 is a valid CAS Registry Number.
62574-65-6Relevant academic research and scientific papers
Nucleophilic solvent participation in the solvolysis of tertiary bromoalkanes
Liu, Kwang-Ting,Hou, Su-Jiun,Tsao, Meng-Lin
body text, p. 425 - 430 (2009/12/24)
The solvolysis of 2-bromo-2-methylpropane (1B), 2-bromo-2-methylbutane (2B), 2-bromo-2,3-dimethylbutane (3B), 2-bromo-2,3,3-trimethylbutane (4B), 3-bromo-3-methylpentane (5B), 3-bromo-2,3-dimethylpentane (6B), 3-bromo-2,2,3-trimethylpentane (7B), 3-bromo-3-ethylpentane (8B), 3-bromo-3-ethyl-2-methylpentane (9B) and 2-bromo-2,4,4-trimethylpentane (11B) in 15 to 21 solvents was studied, and correlation analyses by using the single- and dual-parameter Grunwald-Winstein equations (Eqns 1 and 2) were examined. Substrates 7B, 9B and 11B showed excellent linear relationship (R ≥ 0.997) in the logk - YBr plots and indicated limiting SN1 mechanism for the solvolysis. On the other hand, bromides 1B-6B and 8B gave linear correlations (R = 0.987-0.996) with the dual-parameter (YBr and NOTs) equation (2) only, which indicated the presence of significant nucleophilic solvent participation. Normal trends of reactivity due to the relief of B-strain could be found in the poorly nucleophilic trifluoroethanol. Similar to the corresponding chlorides, the overwhelming influence of nucleophilic solvent assistance results in the observed inverse order of reactivity: k(2B) > k(3B), k(5B) > k(6B) and k(8B) > k(9B).
