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Usage

Uses

Used in Organic Synthesis and Pharmaceutical Production:
1-methyl-4-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)sulfonyl]benzene is utilized as a building block in organic synthesis, contributing to the creation of new compounds with potential applications in various industries. In pharmaceutical production, it serves as a key intermediate for the synthesis of drugs, leveraging its unique chemical properties to facilitate the development of novel therapeutic agents.
Used as a Flavoring Agent in Food Products:
In the food industry, 1-methyl-4-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)sulfonyl]benzene is employed as a flavoring agent, imparting specific taste profiles to food products. Its ability to enhance flavors and contribute to the overall sensory experience of food makes it a valuable ingredient in the culinary world.
Used in Chemical and Biochemical Research:
The distinctive structure and properties of 1-methyl-4-[(3,7,11-trimethyldodeca-2,6,10-trien-1-yl)sulfonyl]benzene make it an important subject for further research and development in the fields of chemistry and biochemistry. Its potential applications in these areas are vast, ranging from the discovery of new chemical reactions to the exploration of its interactions with biological systems.

Upstream product

• 106-28-5 Farnesol 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 24163-93-7 farnesyl bromide 
• 24163-93-7 farnesyl bromide 
• 6784-45-8 (2E,6E)-farnesyl chloride 
• 56194-28-6 3,7,11-trimethyl-2ξ,6E,10-dodecatrien-1-ol 

Downstream Products

• 66958-36-9 1-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyl-29-(toluene-4-sulfonyl)-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-3,4-dimethoxy-2,5-bis-methoxymethoxy-6-methyl-benzene 
• 66958-32-5 1,4-Bis-benzyloxy-2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-29-(toluene-4-sulfonyl)-tetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methyl-benzene 
• 929078-75-1 trimethyl-[7,11,15-trimethyl-5-(toluene-4-sulfonyl)-hexadeca-6,10,14-trien-2-ynyl]-silane 
• 22488-05-7 (2Z,6Z,10E,14E)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaen-1-ol 
• 68690-48-2 1-Methyl-4-((2Z,6Z,10E,14E)-3,7,11,15,19-pentamethyl-icosa-2,6,10,14,18-pentaene-1-sulfonyl)-benzene 
• 92464-90-9 9-(R/S)-p-toluenesulfonyl-3,7,11,15,19,23,27-heptamethyloctaeicosa-2Z,6Z,10Z,14Z,18E,22E,26-heptaen-1-ol benzyl ether 
• 68690-52-8 9-(R/S)-p-toluenesulfonyl-3,7,11,15,19-pentamethyleicosa-2Z,6Z,10E,14E,18-pentaen-1-ol benzyl ether 
• 64634-91-9 1-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-yl]-3,4-dimethoxy-2,5-bis(methoxymethoxy)-6-methylbenzene 
• 111-02-4 2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 
• 39776-45-9 menahydroquinone-4 
• 863-61-6 menatetrenone 
• 94828-03-2 2-(5'-p-tosyl-tetraprenyl)-3-methyl-1,4-dibenzyloxynaphthalene 
• 92542-06-8 1-((6E,10E,14Z,18Z,22Z)-24-Benzyloxy-2,6,10,14,18,22-hexamethyl-tetracosa-2,6,10,14,18,22-hexaene-12-sulfonyl)-4-methyl-benzene 

Relevant academic research and scientific papers

Synthesis of a comprehensive polyprenol library for the evaluation of bacterial enzyme lipid substrate specificity

Polyprenols, a universal class of glycan-carrier lipids, play important roles in glycan biosynthesis in wide variety of living organisms. The chemical synthesis of natural polyisoprenols such as undecaprenol and dolichols, and even more so the synthesis o

Staphylococcus aureus penicillin-binding protein 2 can use depsi-lipid ii derived from vancomycin-resistant strains for cell wall synthesis

Vancomycin-resistant Staphylococcus aureus (S. aureus) (VRSA) uses depsipeptide-containing modified cell-wall precursors for the biosynthesis of peptidoglycan. Transglycosylase is responsible for the polymerization of the peptidoglycan, and the penicillin-binding protein 2 (PBP2) plays a major role in the polymerization among several transglycosylases of wild-type S. aureus. However, it is unclear whether VRSA processes the depsipeptide-containing peptidoglycan precursor by using PBP2. Here, we describe the total synthesis of depsi-lipid I, a cell-wall precursor of VRSA. By using this chemistry, we prepared a depsi-lipid II analogue as substrate for a cell-free transglycosylation system. The reconstituted system revealed that the PBP2 of S. aureus is able to process a depsi-lipid II intermediate as efficiently as its normal substrate. Moreover, the system was successfully used to demonstrate the difference in the mode of action of the two antibiotics moenomycin and vancomycin. Copyright

Stereo- and regioselective synthesis of squalene tetraepoxide

(Chemical Equation Presented) Squalene tetraepoxide, a putative biosynthetic precursor to a variety of oxacyclic triterpenoid natural products, has been efficiently synthesized by anionic coupling of two farnesol-derived diepoxides, which have arisen from

Total syntheses of durgamone, nakorone, and abudinol B via biomimetic oxa- and carbacyclizations

The first biomimetic total syntheses of ent-nakorone, ent-durgamone, and ent-abudinol B were accomplished by combining features of tandem polyepoxide cyclization with biomimetic polyene cyclization. The present biomimetic synthesis route offers efficient