1392804-41-9 Usage
General Description
cis-Methyl 2,2-diMethyl-3-hydroxycyclobutanecarboxylate is a chemical compound with the molecular formula C9H16O3. It is a derivative of cyclobutanecarboxylic acid and is commonly used as a building block in organic synthesis. cis-Methyl 2,2-diMethyl-3-hydroxycyclobutanecarboxylate is characterized by its compact cyclic structure and has been studied for its potential use in pharmaceuticals and agrochemicals. It is also known for its high reactivity and ability to undergo various chemical reactions, making it a versatile compound for the creation of new molecules and materials. Additionally, it is important to note that the "cis" prefix in its name indicates that the two identical substituents on the cyclobutane ring are on the same side of the molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 1392804-41-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,8,0 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1392804-41:
(9*1)+(8*3)+(7*9)+(6*2)+(5*8)+(4*0)+(3*4)+(2*4)+(1*1)=169
169 % 10 = 9
So 1392804-41-9 is a valid CAS Registry Number.
1392804-41-9Relevant articles and documents
Differential oxidation conditions of substituted cyclobutanols derived from terpenes
Kuran, Juan A. Caturelli,Moglioni, Albertina G.
, p. 2393 - 2400 (2014/07/22)
The use of different oxidants for homochiral cyclobutanols afforded dissimilar products depending on the agent used. Dess-Martin periodinane allowed us to obtain the homochiral cyclobutanones and sodium hypochlorite produced only one of the two possible regioisomeric γ-butyrolactones. Copyright
Stereoselective synthesis of chiral precursors to cyclobutane carbocyclic nucleosides and oligopeptides
Rouge, Pablo D.,Moglioni, Albertina G.,Moltrasio, Graciela Y.,Ortuno, Rosa M.
, p. 193 - 196 (2007/10/03)
Versatile and highly efficient synthetic routes leading to optically active cyclobutanones, γ-amino acids and δ-amino alcohols are described. These compounds are relevant synthetic precursors to enantiopure cyclobutane carbocyclic nucleosides and oligopeptides. (-)-(S)-Verbenone is the chiral starting material used and the key synthetic steps involve concerted rearrangements in acidic medium.
