105902-68-9 Usage
Type
Organic compound
A carbon-based molecule with a specific structure and properties.
Functional Groups
Ketone and Nitro group
Ketone
A carbonyl group (C=O) bonded to an alkyl or aryl group (in this case, a hexyl group).
Nitro group
A functional group consisting of an oxygen and nitrogen atom (-NO2) attached to an aryl group (in this case, a phenyl group).
Usage
Industrial solvent
Commonly used in the manufacturing of paints, coatings, and adhesives.
Odor
Sweet and fruity
A pleasant and aromatic scent that can be detected at low concentrations.
Flammability
Flammable
Capable of igniting and burning, posing a fire hazard.
Health Risks
Potentially harmful if inhaled, swallowed, or absorbed through the skin
Can cause adverse health effects if it enters the body through respiratory, digestive, or dermal routes.
Handling and Storage
Handle with caution and store in a cool, well-ventilated area away from heat and open flame
Proper care and precautions should be taken to prevent accidents and minimize exposure to the chemical.
Personal Protective Equipment (PPE)
Wear appropriate PPE when working with this chemical
Necessary to protect the individual from potential health risks associated with the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 105902-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105902-68:
(8*1)+(7*0)+(6*5)+(5*9)+(4*0)+(3*2)+(2*6)+(1*8)=109
109 % 10 = 9
So 105902-68-9 is a valid CAS Registry Number.
105902-68-9Relevant academic research and scientific papers
Palladium-catalyzed synthesis of aryl ketones from boronic acids and carboxylic acids activated in situ by pivalic anhydride
Goossen, Lukas J.,Ghosh, Keya
, p. 3254 - 3267 (2007/10/03)
A new palladium-catalyzed cross-coupling reaction between arylboronic acids and mixed anhydrides, generated in situ from carboxylic acids and pivalic anhydride, is presented. Optimization of the new catalyst and the reaction conditions led to the development of a convenient one-pot ketone synthesis directly from carboxylic and boronic acids in the presence of different (phosphane)palladium complexes in wet THF at 60 °C. Systematic studies were performed to elucidate the reaction mechanism of this transformation. The scope and the limitations of the new process are demonstrated by the synthesis of 33 functionalized ketones. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
