64357-69-3 Usage
Description
(4-cyclohexylphenyl)(phenyl)methanone, also known as 4-Cyclohexylbenzophenone, is a chemical compound with the molecular formula C19H18O. It is a white powder that is commonly used as a UV absorber in various plastics and polymer applications.
Uses
Used in Plastics and Polymer Industry:
(4-cyclohexylphenyl)(phenyl)methanone is used as a UV absorber for protecting plastics and polymers from the harmful effects of ultraviolet radiation, thereby enhancing their durability and stability.
Used in Printing and Coating Industry:
(4-cyclohexylphenyl)(phenyl)methanone is used as a photoinitiator in UV-curable inks and coatings, enabling rapid curing and providing excellent adhesion and durability.
Used in Pharmaceutical and Agrochemical Industry:
(4-cyclohexylphenyl)(phenyl)methanone has potential applications in the production of pharmaceuticals and agrochemicals, where it can be utilized as an intermediate or a key component in the synthesis of various active ingredients.
It is important to handle this chemical with care and to follow proper safety precautions when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 64357-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,5 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64357-69:
(7*6)+(6*4)+(5*3)+(4*5)+(3*7)+(2*6)+(1*9)=143
143 % 10 = 3
So 64357-69-3 is a valid CAS Registry Number.
64357-69-3Relevant articles and documents
Nickel-catalyzed C-N bond activation: Activated primary amines as alkylating reagents in reductive cross-coupling
Yue, Huifeng,Zhu, Chen,Shen, Li,Geng, Qiuyang,Hock, Katharina J.,Yuan, Tingting,Cavallo, Luigi,Rueping, Magnus
, p. 4430 - 4435 (2019/04/29)
Nickel-catalyzed reductive cross coupling of activated primary amines with aryl halides under mild reaction conditions has been achieved for the first time. Due to the avoidance of stoichiometric organometallic reagents and external bases, the scope regarding both coupling partners is broad. Thus, a wide range of substrates, natural products and drugs with diverse functional groups are tolerated. Moreover, experimental mechanistic investigations and density functional theory (DFT) calculations in combination with wavefunction analysis have been performed to understand the catalytic cycle in more detail.
BIS(TRI-n-BUTYLSTANNYL)BENZOPINACOLATE: PREPARATION AND USE AS A MEDIATOR OF INTERMOLECULAR FREE RADICAL REACTIONS
Hart, David J.,Krishnamurthy, Ramanarayanan,Pook, Lori M.,Seely, Franklin L.
, p. 7819 - 7822 (2007/10/02)
Bis(tri-n-butylstannyl)benzopinacolinate (2) serves as a thermal source of tri-n-butylstannyl radicals and mediates intermolecular coupling of selected alkyl halides to O-benzylformaldoxime and electron deficient olefins.A free radical non-chain mechanism is proposed for these reactions.