76334-30-0

Basic information

• Product Name: 9-Iodo-1-nonanol
• Synonyms: 9-Iodo-1-nonanol;9-Iodononan-1-ol
• CAS NO: 76334-30-0
• Molecular Formula: C₉H₁₉IO
• Molecular Weight: 270
• Mol File: 76334-30-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 9-Iodo-1-nonanol(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Iodo-1-nonanol(76334-30-0)
• EPA Substance Registry System: 9-Iodo-1-nonanol(76334-30-0)

Safety Data

• Hazardous Substances Data: 76334-30-0(Hazardous Substances Data)

Usage

General Description

9-Iodo-1-nonanol is a chemical compound with the molecular formula C9H19IO. It is an iodinated derivative of 1-nonanol, meaning it consists of a 1-nonanol molecule with an iodine atom attached to it. 9-Iodo-1-nonanol is commonly used as a reagent in organic synthesis, particularly for the preparation of iodinated organic compounds. It is also utilized in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Additionally, 9-Iodo-1-nonanol has applications in the field of neuroscience and is used to study the effects of iodine-containing compounds on various biological processes. Due to its unique chemical structure and properties, 9-Iodo-1-nonanol has important applications in a wide range of scientific and industrial fields.

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 articles and documents

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.

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.

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.