625-67-2 Usage
Uses
Used in Chemical Synthesis:
2,4-Dichloropentane is used as an intermediate in the synthesis of other organic compounds, facilitating the creation of a wide range of chemical products that are essential in various industries.
Used as a Solvent in Industrial Processes:
In various industrial applications, 2,4-dichloropentane is utilized as a solvent due to its ability to dissolve a broad spectrum of substances, which is crucial for processes such as cleaning, degreasing, and the manufacturing of certain products.
Used in Organic Chemistry Reactions:
2,4-Dichloropentane is employed as a reagent in organic chemistry, particularly for its role in the formation of carbon-carbon bonds, which is a fundamental aspect of creating complex organic molecules.
Used in Pharmaceutical Industry:
2,4-Dichloropentane may be used in the pharmaceutical industry as a component in the synthesis of various drugs, given its ability to participate in key chemical reactions that lead to the development of medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dichloropentane could be utilized in the production of pesticides and other agricultural chemicals, where its properties as a chlorinated hydrocarbon are advantageous for specific chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 625-67-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 625-67:
(5*6)+(4*2)+(3*5)+(2*6)+(1*7)=72
72 % 10 = 2
So 625-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H10Cl2/c1-4(6)3-5(2)7/h4-5H,3H2,1-2H3
625-67-2Relevant academic research and scientific papers
Flexible molecules with defined shape XI[≠]. - Conformer equilibria in 2,4-disubstituted pentane derivatives
Hoffmann, Reinhard W.,Stenkamp, Dirk,Trieselmann, Thomas,G?ttlich, Richard
, p. 2915 - 2927 (2007/10/03)
2,4-Disubstituted penfanes are molecules which adopt essentially only two conformations. Substituents have been varied in order to find those which lead to a strong preference of the conformer equilibrium. Studying 2- substituted 4-methylpentanes 3 and 4-benzyloxypentanes 12, it has been shown that substituent effects on the conformer equilibria are not additive, as would be expected on the grounds of steric effects alone. Rather, interactions between polar groups reinforce the bias of the conformer equilibria. When applied to 2,4-disubstituted pentanes, substituents such as chloro or phthalimido shift the conformer equilibrium to the side of the gg conformer with preferences exceeding 90%.
