23107-52-0 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(hydroxymethyl)cyclobutan-1-one is used as a key intermediate for the synthesis of various pharmaceuticals. Its unique cyclic structure and reactivity make it a valuable component in the development of new drugs.
Used in Agricultural Chemical Production:
2-(hydroxymethyl)cyclobutan-1-one is used as a starting material in the production of agricultural chemicals. Its versatility allows for the creation of effective compounds for pest control and crop protection.
Used as a Solvent:
2-(hydroxymethyl)cyclobutan-1-one is used as a solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it a useful component in many industrial applications.
Used in Chemical Production:
2-(hydroxymethyl)cyclobutan-1-one is used as a building block in the production of other chemicals. Its reactivity and cyclic structure contribute to the synthesis of a variety of chemical compounds.
Used in Fragrance and Flavor Manufacturing:
2-(hydroxymethyl)cyclobutan-1-one is used in the manufacturing of fragrances and flavors for various consumer products. Its sweet and fruity odor makes it a desirable component in creating appealing scents and tastes.
Check Digit Verification of cas no
The CAS Registry Mumber 23107-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23107-52:
(7*2)+(6*3)+(5*1)+(4*0)+(3*7)+(2*5)+(1*2)=70
70 % 10 = 0
So 23107-52-0 is a valid CAS Registry Number.
23107-52-0Relevant academic research and scientific papers
Reaction of dimethoxycarbene with strained cyclic carbonyl compounds
Venneri,Warkentin
, p. 1194 - 1203 (2007/10/03)
A cyclopropanone, a cyclopropenone, cyclobutanones, a cyclobutane-1,3-dione, and a cyclobutene-1,2-dione reacted with dimethoxycarbene to afford acetals of the next larger ring by formal insertion of the carbene into a C-C bond α to the carbonyl group. When either of two saturated α-ring carbons could be involved in the process, the ring expansion was selective, affording primarily the product of apparent insertion into the more substituted ring bond. With 2,3-dimethoxycyclobutene-1,2-dione, insertion occurred between the carbonyl groups and with β-propiolactone it occurred at the lactone bond. β-Propiolactam, however, reacted by insertion of the carbene into the N-H bond.
Cyclopropanones. Formation of Vinylcyclopropanols and Their Rearrangement to Cyclobutanones
Wasserman, Harry H.,Hearn, Michael J.,Cochoy, Robert E.
, p. 2874 - 2880 (2007/10/02)
Vinylcyclopropanols, formed by the addition of vinylmagnesium bromide to the ethyl hemiketal of cyclopropanone, may be converted to cyclobutanone derivatives on reaction with various electrophiles.The ring enlargement of 1-vinyl-2-methylcyclopropanol takes place by preferential migration of the more highly substituted carbon atom.
