1118-00-9 Usage
Uses
Used in Chemical Industry:
1-Methoxy-2,2-dimethylpropane is used as a solvent for various industrial applications, including the production of paints, coatings, and adhesives. Its solubility properties make it suitable for dissolving a wide range of substances, facilitating chemical reactions and processes.
Used in Pharmaceutical Industry:
1-Methoxy-2,2-dimethylpropane is used as a solvent in the synthesis of pharmaceutical compounds. Its ability to dissolve a variety of substances aids in the production of drugs and medications, contributing to the development of new treatments and therapies.
Used in Laboratory Research:
1-Methoxy-2,2-dimethylpropane is utilized as a solvent in laboratory research for the analysis and testing of various chemical compounds. Its properties allow for accurate and efficient experimentation, contributing to scientific advancements and discoveries.
Used in Cleaning Agents:
1-Methoxy-2,2-dimethylpropane is employed as a component in cleaning agents and degreasers due to its ability to dissolve grease, oil, and other contaminants. Its effectiveness in removing dirt and grime makes it a valuable component in various cleaning products.
Used in Fuel Additives:
1-Methoxy-2,2-dimethylpropane is used as a fuel additive to improve the performance and efficiency of gasoline. Its properties help to reduce engine knocking and increase the octane rating, providing a more stable and powerful combustion process.
Check Digit Verification of cas no
The CAS Registry Mumber 1118-00-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1118-00:
(6*1)+(5*1)+(4*1)+(3*8)+(2*0)+(1*0)=39
39 % 10 = 9
So 1118-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O/c1-6(2,3)5-7-4/h5H2,1-4H3
1118-00-9Relevant academic research and scientific papers
Photoinduced Electron Transfer Initiated Activation of Organoselenium Substrates as Carbocation Equivalents: Sequential One-Pot Selenylation and Deselenylation Reaction
Pandey, Ganesh,Soma Sekhar, B. B. V.
, p. 7367 - 7372 (2007/10/02)
The investigation presented in this paper explores the mechanistic aspects and synthetic potentials of PET activation of organoselenium substrates.Fluorescence quenching of 1DCN* by a number of organoselenium compounds (RCH2SeR', 1-4), correlation of the fluorescence quenching rate constants with the oxidation potentials of 1-4, and the dependence of photodissociation quantum yields of 1-4 on their concentration suggests the occurence of electron transfer processes between 1DCN* and 1-4.Steady-state photolysis of 1-4 in the presence of 1DCN* leads to the efficient one-electron oxidative heterolytic dissociation of the carbon-selenium bond to produce the carbocation (RCH2(1+) or equivalent) and radical-centered selenium species (R'Se(.)) via the intermediacy of cation-radical .Nucleophilic assistance in the fragmentation of (RCH2SeR')(1+.) by methanol has been suggested on the basis of products obtained from the control PET reaction of neopentyl phenyl selenide (8).The synthetic utility of these findings has been demonstrated for the deselenylation (Table 4) as well as one-spot sequential selenylation-deselenylation (Table 5) reactions.
