23153-61-9 Usage
Uses
Used in Organic Synthesis:
(2,2-diethoxycyclobutyl)methanol is used as a building block in organic synthesis for the creation of various other organic compounds. Its unique structure allows it to be a versatile component in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
(2,2-diethoxycyclobutyl)methanol is used as an intermediate in the preparation of pharmaceuticals. Its reactivity and unique structure make it a valuable component in the development of new drugs and medications.
Used in Agrochemical Industry:
(2,2-diethoxycyclobutyl)methanol is used as a precursor in the synthesis of agrochemicals. Its ability to form various organic compounds makes it a useful building block in the development of new agricultural chemicals.
Used in Specialty Chemicals:
(2,2-diethoxycyclobutyl)methanol is used in the production of specialty chemicals. Its unique properties and reactivity contribute to the development of specialized chemical products for various industries.
Used in Laboratory Experiments and Research:
(2,2-diethoxycyclobutyl)methanol is used as a reagent in laboratory experiments and research. Its unique structure and reactivity make it a valuable tool for studying chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 23153-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,5 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23153-61:
(7*2)+(6*3)+(5*1)+(4*5)+(3*3)+(2*6)+(1*1)=79
79 % 10 = 9
So 23153-61-9 is a valid CAS Registry Number.
23153-61-9Relevant 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.
