4110-44-5 Usage
Description
3,3-Dimethyloctane, an alkane with the chemical formula C10H22, is a volatile organic compound and a bacterial as well as plant metabolite. It is derived from octane by replacing the two methylene hydrogens at position 3 with methyl groups. This organic compound has been identified for its potential applications in various fields, particularly due to its ability to inhibit certain biological processes.
Uses
Used in Agricultural Applications:
3,3-Dimethyloctane is used as a bioactive compound for the treatment of nematodes and rhizosphere soils. Its application reason lies in its ability to effectively combat these pests, which can be detrimental to crop health and yield.
Used in Insecticide Formulations:
In the field of pest control, 3,3-dimethyloctane is utilized as an insecticide. The application reason is its demonstrated effectiveness in controlling and managing insect populations, thereby protecting crops and reducing the need for chemical insecticides.
Used in Pharmaceutical Research:
3,3-Dimethyloctane has shown potential in the pharmaceutical industry due to its ability to inhibit the growth of human alveolar cells and root tissues. The application reason is its potential use in developing targeted therapies for specific types of cancer or other diseases where these cell types are involved.
However, it is important to note that 3,3-dimethyloctane does not affect platelet aggregation or exudates, which indicates its selectivity in targeting specific biological processes.
Toxicity Mechanism:
The toxicity of 3,3-dimethyloctane is mediated through its inhibition of mitochondrial electron transport. This inhibition disrupts the normal functioning of cells, leading to cell death by apoptosis or necrosis. Understanding this mechanism can help in the development of safer and more effective applications for this compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 4110-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4110-44:
(6*4)+(5*1)+(4*1)+(3*0)+(2*4)+(1*4)=45
45 % 10 = 5
So 4110-44-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H22/c1-5-7-8-9-10(3,4)6-2/h5-9H2,1-4H3
4110-44-5Relevant articles and documents
High-performance ring-opening catalysts based on iridium-containing zeolite Beta in the hydroconversion of decalin
Santi, Dominic,Holl, Tobias,Calemma, Vincenzo,Weitkamp, Jens
, p. 46 - 57 (2013/06/04)
Decalin was converted in a flow-type reactor under a hydrogen pressure of 5.2 MPa on Ir/H,A-Beta zeolite catalysts, where A stands for an alkali metal cation. In one series of catalysts, the Ir content was 3 wt.%, and the nature of A was varied from lithi
IONIC ALKYLATION OF TERTIARY ALKYL HALIDES WITH TETRAALKYLSILANES
Bolestova, G. I.,Parnes, Z. N.
, p. 32 - 36 (2007/10/02)
In the reaction of tertiary alkyl halides with tetraethyl-, tetrapropyl-, tetrabutyl-, and tetraamylsilane in the presence of AlX3 the halogen atom is substituted by the alkyl group with the formation of the corresponding saturated hydrocarbons containing a quaternary carbon atom.As a result of the hydride mobility of the β-hydrogen atom in the tetraalkylsilane ionic hydrogenolysis of the substrate occurs in addition to alkylation, and the degree of hydrogenolysis depends on the alkyl substituent in the silane.
