76334-30-0

Usage

Uses

Used in Organic Synthesis:
9-Iodo-1-nonanol is used as a reagent for the preparation of iodinated organic compounds. Its iodine atom can be incorporated into various organic molecules, providing a versatile building block for the synthesis of a wide range of chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 9-Iodo-1-nonanol serves as a key intermediate in the synthesis of certain drugs. Its unique properties allow for the development of new medications with potential therapeutic benefits.
Used in Agrochemical Production:
9-Iodo-1-nonanol is also utilized in the production of agrochemicals, such as pesticides and herbicides. Its iodine-containing structure can enhance the effectiveness of these chemicals, leading to improved agricultural outcomes.
Used in Specialty Chemicals:
9-Iodo-1-nonanol finds applications in the creation of specialty chemicals, which are tailored for specific industries and applications. The unique properties of 9-Iodo-1-nonanol make it a valuable component in these specialized formulations.
Used in Neuroscience Research:
9-Iodo-1-nonanol has applications in the field of neuroscience, where it is used to study the effects of iodine-containing compounds on various biological processes. Its iodine atom allows researchers to investigate the role of iodine in brain function and neurochemistry, potentially leading to new insights and treatments for neurological disorders.

Upstream product

• 55362-80-6 9-bromononan-1-ol 
• 3937-56-2 1,9-Nonanediol 

Downstream Products

• 2664-55-3 n-nonyl acrylate 
• 76334-21-9 2-allyl-2-(9-hydroxynonyl)cyclohexane-1,3-dione 
• 862700-70-7 3,17β-bis(2-tetrahydropyranyloxy)-7α-[9-(4,4,5,5,5-pentafluoropentyl)thiononyl]estra-1,3,5(10)-triene-6-one 
• 153004-31-0 (+)-(7α)-[9-(4,4,5,5,5-pentafluoropentylsulfanyl)nonyl]estra-1,3,5(10)-triene-3,17β-diol 
• 129453-61-8 fulvestrant 
• 511545-94-1 9-(4,4,5,5,5-pentafluoropentylsulfanyl)nonyl alcohol 

Relevant academic research and scientific papers

Processes and intermediates for preparing fulvestrant

The present invention provides a method and an intermediate for preparing fulvestrant, and relates to a method for preparing fulvestrant, and an intermediate (5) of fulvestrant, and a synthetic methodthereof. The method provided by the invention can be used for obtaining high-purity fulvestrant, and is suitable for industrial mass production.

Application of "click" chemistry in solid phase synthesis of alkyl halides

A convenient and highly selective microwave assisted procedure for the conversion of allylic, benzylic and aliphatic alcohols to their corresponding halides using polymer-bound triphenylphosphine and iodine is presented. In case of symmetrical diols, mono-iodination product is obtained in very high yield. Additionally, highly regioselective behavior is observed in our procedure. Simplicity in operation, no column chromatography required for the purification of the products, recyclability of the reagents used, short reaction times and good to excellent yields are the advantages of our protocol. Most functional groups remain unaffected under our reaction condition.

Synthesis and physical properties of ferrocene derivatives (XXV) liquid crystallinity of 1,3-disubstituted ferrocene derivatives

Liquid crystallinity of 1,3-disubstituted ferrocene derivatives was studied by DSC and polarizing microscope. The name of the derivatives is 1,3-bis[-[4-(4-methoxyphenoxycarbonyl)phenoxy]alkyloxycarbonyl]ferrocene. Nine members from n = 2 to 10 were synthesized (n is carbon number of alkyl chain in the sample). All samples except n = 2 and 4 exhibited monotropic nematic liquid crystalline phase. In addition, smectic X (not yet completely identified) was also observed in n = 8 and 10. Liquid crystalline phase transition phenomena were discussed from a viewpoint of molecular shape. Copyright Taylor & Francis Group, LLC.

Synthesis and physical properties of ferrocene derivatives (XXIII): Phase transition and unique molecular structure of monosubstituted ferrocene derivatives

The monosubstituted ferrocene derivatives, -[4-(4-methoxyphenoxycarbonyl) phenoxy]alkoxycarbonyl ferrocene, were synthesized in order to compare the liquid crystallinity to that of disubstituted ferrocene derivatives, 1,1'-bis[-[4-(4-methoxy-phenoxycarbonyl)phenoxy]alkoxycarbonyl]ferrocene. Some of the monosubstituted ferrocene derivatives containing relatively longer flexible spacer showed the liquid crystalline phase, nematic and/or smectic phases. The crystal structure of 2-[4-(4-methoxyphenoxycarbonyl)phenoxy] ethoxycarbonyl ferrocene was determined by X-ray diffraction method using a single crystal. The molecular structure revealed a bent structure that is almost a half of "Z" shaped molecular structure of 1,1'-bis[2-[4-(4- methoxyphenoxycarbonyl)phenoxy]ethoxycarbonyl]ferrocene.

A New Synthetic Method of Macrocyclic Lactones from ω-Iodoalkylacrylates

When the photostimulated cyclization reaction of ω-iodoalkylacrylates was performed in the presence of metal hydride complexes such as sodium cyanoborohydride (NaBH3CN), sodium borohydride (NaBH4) and potassium borohydride (KBH4), the corresponding macrocyclic lactones were produced.The use of NaBH3CN led to the highest yield of lactones.