35883-77-3

Usage

Uses

Used in Industrial Applications:
Cyclohexanone, 4-(phenylmethyl)is used as a solvent for various manufacturing processes, including the production of nylon and other synthetic fibers.
Used in Pharmaceutical Applications:
Due to its unique properties conferred by the 4-(phenylmethyl) substitution, Cyclohexanone, 4-(phenylmethyl)may be used as a precursor or intermediate in the synthesis of pharmaceutical compounds.
Used in Agrochemical Applications:
Cyclohexanone, 4-(phenylmethyl)-'s additional properties may also make it useful in the development of agrochemicals, although further research and testing is necessary to fully understand its potential uses in this industry.
However, due to its aromatic nature, Cyclohexanone, 4-(phenylmethyl)may pose health and environmental hazards and require special handling and disposal procedures. Further research and testing is likely necessary to fully understand the potential uses and risks associated with this chemical.

Upstream product

• 101-53-1 p-benzylphenol 
• 176972-48-8 4-benzylcyclohexanol 
• 64-19-7 acetic acid 
• 153788-41-1 4-benzyl-1-trimethylsilyloxylbicyclo<3.1.0>hexane 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 69225-59-8 3,3-dimethyl-1,5-dioxaspiro[5.5]undecan-9-one 
• 1589-82-8 phenylmagnesium bromide 
• 83631-87-2 8-Benzylidene-1,4-dioxa-spiro[4.5)decane 
• 1449-46-3 benzyltriphenylphosphonium bromide 
• 4746-97-8 cyclohexanedione monoethylene ketal 
• 607744-45-6 8-benzyl-1,4-dioxaspiro[4.5]decan-8-ol 
• 83631-88-3 8-benzyl-1,4-dioxaspiro[4.5]decane 
• 221533-40-0 8-(4-chlorobenzylidene)-1,4-dioxaspiro<4.5>decane 
• 873-76-7 para-Chlorobenzyl alcohol 

Downstream Products

• 54576-12-4 3-benzyl-adipic acid 
• 75930-69-7 4-benzyl-1-<(N-methylcarbamoyl)benzyl>cyclohexanol 
• 75930-66-4 4-benzylspiro(cyclohexanone-1,3'-isochroman)-1'-one 
• 86727-14-2 4-(4-benzylcyclohexylidene)isochroman 
• 35883-78-4 3-(4-oxo-1,2,3,4-tetrahydro-[2]naphthyl)-propionic acid 
• 337970-59-9 2-(4-Benzyl-cyclohexylidenemethyl)-1H-benzimidazole 
• 338970-85-7 1-(4-benzyl-cyclohex-1-enyl)-pyrrolidine 
• 1023309-38-7 C₁₃H₁₈O₄ 

Relevant academic research and scientific papers

Desymmetrizing Isomerization of Alkene via Thiazolinyl Iminoquinoline Cobalt Catalysis

We report a cobalt-catalyzed desymmetrizing isomerization of exo-cyclic alkenes to generate chiral 1-methylcyclohexene derivatives with good yields and enantioselectivities. A novel chiral thiazolinyl iminoquinoline ligand and its cobalt complex were desi

Cobalt-Catalyzed Desymmetric Isomerization of Exocyclic Olefins

Chiral cyclic olefins, 1-methylcyclohexenes, are versatile building blocks for the synthesis of pharmaceuticals and natural products. Despite the prevalence of these structural motifs, the development of efficient synthetic methods remains an unmet challenge. Herein we report a novel desymmetric isomerization of exocyclic olefins using a series of newly designed chiral cobalt catalysts, which enables a straightforward construction of chiral 1-methylcyclohexenes with diversified functionalities. The synthetic utility of this methodology is highlighted by a concise and enantioselective synthesis of a natural product, β-bisabolene. The versatility of the reaction products is further demonstrated by multifarious derivatizations.

SELECTIVE LIGANDS OF HUMAN CONSTITUTIVE ANDROSTANE RECEPTOR

The present invention provides a structurally novel class of heterocyclic compounds of general formula I wherein L1 is heteroaryl and L2 is heteroaryl or aryl. The novel compounds are useful in a method of prevention or treatment of a condition which is m

PARTIALLY SATURATED NITROGEN-CONTAINING HETEROCYCLIC COMPOUND

There are provided compounds having a superior PHD2 inhibitory effect that are represented by general formula (I'): (in the above-mentioned general formula (I'), W, Y, R2, R3, R4, and Y4 are as described hereinabove), or pharmaceutically acceptable salts thereof.

An efficient route into synthetically challenging bridged achiral 1,2,4,5-tetraoxanes with antimalarial activity

Here we present an efficient route into synthetically challenging bridged 1,2,4,5-tetraoxanes. The key to the success of this route is the use of H2O2 and catalytic I2 to form the gem-dihydroperoxide followed by a Ag2

COMPOUNDS FOR INHIBITING KSP KINESIN ACTIVITY

The present invention provides compounds of Formula (I) (wherein R1, R3, X, W, Z and ring Y are as defined herein). The present invention also provides compositions comprising these compounds that are useful for treating cellular proliferative diseases or disorders associated with KSP kinesin activity and for inhibiting KSP kinesin activity.

Synthesis of cyclopropyl silyl ethers and their facile ring opening by photoinduced electron transfer as key step in radical/radical cationic cascade reactions

Various ring-fused cyclopropyl silyl ethers with an benzylic, olefinic or acetylenic side chain have been synthesized. Upon oxidative photoinduced electron transfer (PET) the cyclopropane ring opens and forms a reactive β-keto radical, which undergoes intramolecular cyclization. In some cases we observed only formation of ring opened non-cyclized products. With olefinic side chain 5-exo-trig mode of cyclization rather than 6-endo-trig mode of cyclization takes place whereas in case of acetylenic side chain we observed 6-endo cyclization.

2-Cyclohexyl quinazoline NMDA/NR2B antagonists

4-substituted cyclohexanes substituted in the 1-position with quinazoline either directly or through a C1-C4alkyl, C1-C4alkenyl, C1-C4alkynyl, C1-C4alkoxy, amino, amin

2-CYCLOHEXYL IMIDAZOPYRIDINE NMDA/NR2B ANTAGONISTS

4-substituted cyclohexanes substituted in the 1-position with imidazopyridine either directly or through a C1-C4alkyl, C1-C4alkenyl, C1-C4alkynyl, C 1-C4alkoxy, amino, aminoC1-C4alkyl, hydroxyC1-C4alkyl, carbonyl, cycloC3-C 6alkyl or aminocarbonyl chain a

5-benzyl-octahydroindole and 6-benzyl-decahydroquinoline NMDA/NR2B antagonists

Novel 5-benzyl-octahydroindoles and 6-benzyl-decahydroquinolines substituted in the 1-position are effective as NMDA NR2B antagonists useful for relieving pain.