25346-31-0 Usage
Uses
Used in Pharmaceutical Industry:
3-Bromo-3-methylpentane is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique structure allows for the creation of complex molecules that can target specific biological pathways, leading to the development of more effective treatments for a range of diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 3-bromo-3-methylpentane is utilized as a precursor in the synthesis of pesticides and other crop protection agents. Its incorporation into these products helps to enhance their effectiveness in controlling pests and diseases, thereby improving crop yields and food security.
Used in Manufacturing Industry:
3-Bromo-3-methylpentane also serves as a solvent in the manufacturing of various products such as adhesives, paints, and coatings. Its solvent properties enable the formation of stable and durable formulations, which are essential for the performance and longevity of these products.
Safety Precautions:
Given its moderately hazardous nature, 3-bromo-3-methylpentane should be handled with care due to its flammability and potential health hazards. It is crucial to follow proper safety precautions, including the use of personal protective equipment, when handling and storing this chemical to minimize the risk of accidents and exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 25346-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,4 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25346-31:
(7*2)+(6*5)+(5*3)+(4*4)+(3*6)+(2*3)+(1*1)=100
100 % 10 = 0
So 25346-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H13Br/c1-4-6(3,7)5-2/h4-5H2,1-3H3
25346-31-0Relevant articles and documents
Nucleophilic solvent participation in the solvolysis of tertiary bromoalkanes
Liu, Kwang-Ting,Hou, Su-Jiun,Tsao, Meng-Lin
, p. 425 - 430 (2009)
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).
