6635-68-3 Usage
Uses
Pharmaceutical manufacturing, fragrances, and flavoring agents 1-cyclopentylbutan-1-one serves as a key ingredient or intermediate in the production of various medicines, scents, and taste-enhancing substances.
Physical state
Colorless liquid It is a transparent liquid without any color.
Odor
Sweet, fruity The compound has a pleasant and characteristic aroma reminiscent of sweet fruits.
Versatility
Building block for organic synthesis It is commonly used as a starting material or intermediate in the synthesis of a wide range of organic compounds.
Solvent
Chemical processes 1-Cyclopentylbutan-1-one is often employed as a solvent in various chemical reactions and processes.
Flammability
Flammable The compound can easily catch fire and pose fire and explosion hazards.
Safety precautions
Handle and store with caution It is essential to follow proper safety protocols and regulations when working with 1-Cyclopentylbutan-1-one to prevent accidents and ensure safe handling.
Check Digit Verification of cas no
The CAS Registry Mumber 6635-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6635-68:
(6*6)+(5*6)+(4*3)+(3*5)+(2*6)+(1*8)=113
113 % 10 = 3
So 6635-68-3 is a valid CAS Registry Number.
6635-68-3Relevant academic research and scientific papers
A NEW SYNTHESIS OF KETONES FROM 1,2-DIMETHOXYETHENYLLITHIUM, ORGANOBORANES, AND ALKYL FLUOROSULFONATES
Yogo, Toshinobu,Koshino, Junji,Suzuki, Akira
, p. 1059 - 1060 (2007/10/02)
The reaction of alkyl fluorosulfonates with lithium 1,2-dimethoxyethenyltrialkylborates readily prepared from organoboranes gives corresponding ketones in good yields.
Reactions of organoboranes and 2-lithio-2-alkyl-1,3-benzodithioles. A new, improved synthesis of ketones
Ncube, Smollie,Pelter, Andrew,Smith, Keith
, p. 1893 - 1894 (2007/10/09)
Reactions of trialkylboranes with 2-lithio-2-alkyl-1,3-benzodithioles followed by oxidation give ketones in good yields. This method is far less subject to steric hindrance than the analogous reactions using anions derived from bis(phenylthio)alkanes.
