1815-99-2

Basic information

• Product Name: 4-N-DECYLPYRIDINE
• Synonyms: 4-N-DECYLPYRIDINE;4-Decylpyridine
• CAS NO: 1815-99-2
• Molecular Formula: C15H25 N
• Molecular Weight: 219.37
• Mol File: 1815-99-2.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 4-N-DECYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-N-DECYLPYRIDINE(1815-99-2)
• EPA Substance Registry System: 4-N-DECYLPYRIDINE(1815-99-2)

Safety Data

• Hazardous Substances Data: 1815-99-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-N-Decylpyridine is utilized as a key building block in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-N-Decylpyridine serves as a crucial component in the creation of pesticides and other agricultural chemicals. Its incorporation into these products enhances their effectiveness in protecting crops and managing pests, thereby supporting sustainable agriculture.
Used in Organic Compounds Synthesis:
4-N-Decylpyridine is employed as a versatile intermediate in the synthesis of a wide range of organic compounds. Its presence in these reactions facilitates the formation of complex molecules with diverse applications across various industries, including materials science, fragrances, and dyes.

Upstream product

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Relevant articles and documents

Cobaloxime-Mediated Radical Alkyl-Heteroaromatic Substitution

The first examples of cobaloxime-mediated radical alkyl-heteroaromatic cross-coupling, replacing a C-H in the protonated heteroaromatic with a C-alkyl, are accomplished via anaerobic visible light photolysis of 95percent EtOH solutions of primary and secondary alkyl cobaloximes, RCoIII(dmgH)2py (dmgH = dimethylglyoxime monoanion), and pyridinium, quinolinium, 4-methylpyridinium, benzothiazolium, and benzimidazolium p-toluenesulfonate.

Nickel-catalyzed alkylative cross-coupling of anisoles with grignard reagents via C-O bond activation

We report nickel-catalyzed cross-coupling of methoxyarenes with alkylmagnesium halides, in which a methoxy group is eliminated. A wide range of alkyl groups, including those bearing β-hydrogens, can be introduced directly at the ipso position of anisole derivatives. We demonstrate that the robustness of a methoxy group allows this alkylation protocol to be used to synthesize elaborate molecules by combining it with traditional cross-coupling reactions or oxidative transformation. The success of this method is dependent on the use of alkylmagnesium iodides, but not chlorides or bromides, which highlights the importance of the halide used in developing catalytic reactions using Grignard reagents.

4-ALKYL SUBSTITUTED PYRIDINES AS ODIFEROUS SUBSTANCES

The present invention primarily concerns certain 4-alkyl pyridines of the following formula (I), wherein R is C8-C12 alkyl, odiferous substance mixtures and aromatic substance mixtures containing these 4-alkyl pyridines, the respective uses thereof as an odiferous or aromatic substance (mixture) and corresponding perfumed products.