102516-18-7 Usage
Description
Ethanone, 1-(2-methoxycyclopropyl)-, trans(9CI) is a unique chemical compound characterized by a cyclopropyl ring attached to a methoxy group on the second carbon of a ketone functional group. The trans configuration signifies that the cyclopropyl and methoxy groups are positioned on opposite sides of the molecule. This distinctive structure and properties may offer potential applications in various industries, particularly pharmaceutical or agrochemical, although further research is necessary to confirm its specific uses and effects. Due to its potential reactivity and toxicity, safety precautions should be exercised during handling and utilization.
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(2-methoxycyclopropyl)-, trans(9CI) is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique structure may contribute to novel therapeutic effects and mechanisms of action, offering new treatment options for various medical conditions. However, further research is required to explore its pharmacological properties, efficacy, and safety profile.
Used in Agrochemical Industry:
Ethanone, 1-(2-methoxycyclopropyl)-, trans(9CI) may also find applications in the agrochemical industry as a potential pesticide or herbicide. Its specific chemical properties could provide new ways to control pests and weeds, enhancing crop protection and yield. However, extensive research and testing are needed to determine its effectiveness, safety, and environmental impact in this context.
Check Digit Verification of cas no
The CAS Registry Mumber 102516-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,1 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102516-18:
(8*1)+(7*0)+(6*2)+(5*5)+(4*1)+(3*6)+(2*1)+(1*8)=77
77 % 10 = 7
So 102516-18-7 is a valid CAS Registry Number.
102516-18-7Relevant articles and documents
A New and Convenient Method of Synthesis of γ-Ketoaldehydes
Kulinkovich, O. G.,Tischenko, I. G.,Sorokin, V. L.
, p. 1058 - 1059 (1985)
A new synthesis of 4-oxoalkanals starting from acid chlorides and allyl chloride proceeding via alkyl 2,3-dichloropropyl ketones, alkyl 3-chloropropenyl ketones, alkyl 3-chloro-2-methoxypropyl ketones, and 1-alkanoyl-2-methoxycyclopropanes is described.
SIMPLE METHOD FOR THE PRODUCTION OF ALKYL TRANS-2-METHOXYCYCLOPROPYL KETONES
Kulinkovich, O. G.,Tishchenko, I. G.,Sorokin, V. L.
, p. 1514 - 1518 (2007/10/02)
Alkyl 3-Chloro-2-methoxypropyl ketones, obtained in three stages from the corresponding alkanoyl chlorides, are converted by the action of an aqueous solution of sodium hydroxide into alkyl trans-2-methoxycyclopropyl ketones.During hydrolysis in a weakly acidic medium the latter form the corresponding γ-keto aldehydes.
