4110-44-5 Usage
Uses
3,3-Dimethyloctane has been shown to be effective in the treatment of nematodes and rhizosphere soils. It can also be used as an insecticide. It has been shown to inhibit the growth of human alveolar cells and root tissues, but not platelet aggregation or exudates. The toxicity of 3,3-dimethyloctane is mediated through its inhibition of mitochondrial electron transport. This inhibition leads to cell death by apoptosis or necrosis.
Definition
ChEBI: 3,3-dimethyloctane is an alkane that is octane in which the two methylene hydrogens at position 3 have been replaced by methyl groups. It has a role as a bacterial metabolite and a plant metabolite. It is an alkane and a volatile organic compound.
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.
