6056-35-5 Usage
Description
2-Benzoyl-5-norbornene is a type of substituted norbornene, which is a compound that contains a norbornene ring moiety and at least one substituent group. It is a clear yellow-orange to brown liquid.
Uses
Used in Chemical Synthesis:
2-Benzoyl-5-norbornene is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for a wide range of chemical reactions, making it a versatile building block in the chemical industry.
Used in Polymer Production:
In the polymer industry, 2-Benzoyl-5-norbornene is used as a monomer for the production of various types of polymers. Its norbornene ring structure provides unique properties to the resulting polymers, such as improved strength and durability.
Used in Pharmaceutical Applications:
2-Benzoyl-5-norbornene may also have potential applications in the pharmaceutical industry. Its chemical structure could be utilized in the development of new drugs or drug delivery systems, although further research would be required to explore these possibilities.
Used in Coatings and Adhesives:
Due to its chemical properties, 2-Benzoyl-5-norbornene can be used as a component in the formulation of coatings and adhesives. Its ability to form strong bonds with other materials makes it a valuable addition to these products.
Used in Lubricants:
The liquid nature of 2-Benzoyl-5-norbornene makes it a potential candidate for use in lubricants. Its chemical properties may provide improved performance and longevity in various applications where lubrication is required.
Used in Dyes and Pigments:
The yellow-orange to brown color of 2-Benzoyl-5-norbornene suggests that it could be used in the production of dyes and pigments. Its unique color properties could be harnessed to create new and innovative colorants for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6056-35-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6056-35:
(6*6)+(5*0)+(4*5)+(3*6)+(2*3)+(1*5)=85
85 % 10 = 5
So 6056-35-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H14O/c15-14(11-4-2-1-3-5-11)13-9-10-6-7-12(13)8-10/h1-7,10,12-13H,8-9H2/t10-,12+,13-/m1/s1
6056-35-5Relevant articles and documents
Exo-selective Diels-Alder reaction based on a molecular recognition approach
Maruoka, Keiji,Imoto, Hiroshi,Yamamoto, Hisashi
, p. 12115 - 12116 (1994)
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Green and Efficient: Iron-Catalyzed Selective Oxidation of Olefins to Carbonyls with O2
Gonzalez-De-Castro, Angela,Xiao, Jianliang
supporting information, p. 8206 - 8218 (2015/07/15)
A mild and operationally simple iron-catalyzed protocol for the selective aerobic oxidation of aromatic olefins to carbonyl compounds is described. Catalyzed by a Fe(III) species bearing a pyridine bisimidazoline ligand at 1 atm of O2, α- and β-substituted styrenes were cleaved to afford benzaldehydes and aromatic ketones generally in high yields with excellent chemoselectivity and very good functional group tolerance, including those containing radical-sensitive groups. With α-halo-substituted styrenes, the oxidation took place with concomitant halide migration to afford α-halo acetophenones. Various observations have been made, pointing to a mechanism in which both molecular oxygen and the olefinic substrate coordinate to the iron center, leading to the formation of a dioxetane intermediate, which collapses to give the carbonyl product. (Chemical Equation).
CHEMOSELECTIVITY IN MOLYBDENUM CATALYZED ALCOHOL AND ALDEHYDE OXIDATIONS
Trost, Barry M.,Masuyama, Yoshiro
, p. 173 - 176 (2007/10/02)
Hydrogen peroxide in the presence of (NH4)6Mo7O24*4H2O and potassium carbonate is a chemoselective method to oxidize secondary alcohols to ketones and to oxidize aldehydes to acids, the latter also accelerated by cerium chloride.
