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Usage

Uses

Used in Fragrance Industry:
(3-METHYL-PENTYL)-BENZENE is used as a fragrance additive for its sweet, floral scent, which imparts a fruity and exotic aroma to consumer products such as perfumes and personal care items.
Used in Specialty Chemicals Production:
(3-METHYL-PENTYL)-BENZENE is used as a raw material in the production of specialty chemicals, contributing to the synthesis of various compounds for different applications.
Used as an Industrial Solvent:
(3-METHYL-PENTYL)-BENZENE is used as a solvent in industrial processes, facilitating the dissolution and interaction of various substances in manufacturing operations.
It is important to handle (3-METHYL-PENTYL)-BENZENE with care, as it may be harmful if ingested or inhaled, and can cause skin and eye irritation upon contact.

Upstream product

• 23033-63-8 (S)-(+)-3-Methyl-1-phenyl-1-pentanon 
• 676-58-4 methylmagnesium chloride 
• 28977-69-7 (S)-3-methylpentanoic acid chloride 
• 1730-92-3 (3S)-methylvaleric acid 
• 534-00-9 (S)-2-methylbutyl bromide 

Downstream Products

• 78976-22-4 (S)-(+)-1-(3-Methylpentyl)-4-nitrobenzol 
• 78976-21-3 (S)-(+)-1-(3-Methylpentyl)-2-nitrobenzol 
• 79027-65-9 cis-(S,S)-(+)-4,4'-Bis(3-methylpentyl)azobenzol 
• 79027-66-0 trans-(S,S)-(+)-4,4'-Bis(3-methylpentyl)azobenzol 
• 78976-10-0 cis-(S,S)-(-)-2,2'-Bis(3-methylpentyl)azobenzol 
• 78976-11-1 trans-(S,S)-(-)-2,2'-Bis(3-methylpentyl)azobenzol 

Relevant academic research and scientific papers

Use of the 2-Pyridinesulfonyloxy Leaving Group for the Fast Copper-Catalyzed Coupling Reaction at Secondary Alkyl Carbons with Grignard Reagents

Investigation of the copper-catalyzed coupling reaction of 2-pyridinesulfonates with Grignard reagents revealed that reactions with catalytic Cu(OTf)2 were completed in 40 min. The results differed from those of the previous CuI-catalyzed reactions of tosylates in the presence of additives (LiOMe and TMEDA) for 12-24 h. It was shown that the preferred coordination of the leaving group to the reagents accelerated the reaction. Successful reagents were MeMgCl and other RMgX. Complete inversion was established.

Synthese chiraler Azobenzole und Untersuchung der in nematischen Fluessigkristallen durch sie induzierten cholesterischen Phasen

The chiral cis- and trans-azo compounds 8a - d and 9a - d with para- or ortho-standing chiral side chains as well as the trans-azoxy derivatives 17a - d and 18a - d are synthesized.The influence of the molecular structure and the distance of the chiral centre from the aromatic nucleus on screw sense and pitch of induced cholesteric phases is investigated.The cis-azo compounds 9c and d show atropisomerism.