129113-06-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Synonyms are alternative names for a chemical compound, often used to describe the same substance in different contexts or by different researchers.
Explanation
The appearance describes the physical state and color of the compound when it is in its pure form.
Explanation
Solubility refers to the ability of a substance to dissolve in a given solvent. In this case, the compound does not dissolve well in water but does dissolve in organic solvents like alcohols, ethers, and hydrocarbons.
Explanation
The compound is used as a reactant in the production of various pharmaceuticals and organic compounds, indicating its importance in the chemical and pharmaceutical industries.
Explanation
The compound's reactivity refers to its ability to undergo chemical reactions with other substances, making it a valuable precursor in the synthesis of other compounds.
Explanation
Due to its reactivity and ability to participate in various chemical reactions, the compound has potential applications in both the pharmaceutical and chemical industries for the development of new products and processes.
Synonyms
3-propyl-1,2-naphthoquinone
Appearance
Yellow solid
Solubility
Insoluble in water, soluble in organic solvents
Uses
Synthesis of pharmaceuticals and organic compounds
Reactivity
Participates in various chemical reactions
Potential Applications
Pharmaceutical and chemical industries
Check Digit Verification of cas no
The CAS Registry Mumber 129113-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,1 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129113-06:
(8*1)+(7*2)+(6*9)+(5*1)+(4*1)+(3*3)+(2*0)+(1*6)=100
100 % 10 = 0
So 129113-06-0 is a valid CAS Registry Number.
129113-06-0Relevant articles and documents
Samarium diiodide-promoted intramolecular ketone-ester coupling reaction: Novel cyclization and ring expansion pathway
Iwaya, Kazuki,Nakamura, Momoe,Hasegawa, Eietsu
, p. 5067 - 5070 (2007/10/03)
When ethyl 2-substituted-1-indanone-2-carboxylates were treated with samarium diiodide (SmI2), ring expansion products such as 3-substituted-1,2-naphthoquinones were isolated. Alcohols were also obtained as the mixture of cis- and trans-isomers of hydroxy and ester substituents. A reaction mechanism involving intramolecular addition of samarium ketyl radicals to ester substituents followed by ring expansion was proposed for the formation of the one-carbon homologated products. Similarly, reaction of ethyl 1-substituted-2-oxo-1-cyclopentanecarboxylates with SmI2 produced 3-substituted-2-hydroxy-2-cyclohexenones along with the corresponding alcohols.
