40145-10-6

Basic information

• Product Name: 6-Iodo-1-Hexanol
• Synonyms: 6-Iodo-1-Hexanol
• CAS NO: 40145-10-6
• Molecular Formula: C₆H₁₃IO
• Molecular Weight: 228.07129
• Mol File: 40145-10-6.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Iodo-1-Hexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Iodo-1-Hexanol(40145-10-6)
• EPA Substance Registry System: 6-Iodo-1-Hexanol(40145-10-6)

Safety Data

• Hazardous Substances Data: 40145-10-6(Hazardous Substances Data)

Usage

General Description

6-Iodo-1-Hexanol is a chemical compound with the molecular formula C6H13IO. It is classified as a haloalcohol, containing both a halogen (iodine) and a hydroxyl group. 6-Iodo-1-Hexanol is a colorless liquid with a strong, pungent odor, and it is commonly used as an intermediate in organic synthesis. It is often employed in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 6-Iodo-1-Hexanol has been studied for its potential use as a reagent in organic reactions such as nucleophilic substitution and palladium-catalyzed cross-coupling reactions. Due to its unique chemical structure and reactivity, 6-Iodo-1-Hexanol is a valuable tool in the field of organic chemistry and has a wide range of industrial applications.

Upstream product

• 629-11-8 1,6-hexanediol 
• 2009-83-8 6-chloro-1-hexanol 
• 4286-55-9 1-bromo-6-hexanol 
• 13159-24-5 ethyl 6-iodohexanoate 
• 1191-25-9 6-Hydroxyhexanoic acid 

Downstream Products

• 19100-93-7 (6-Hydroxyhexyl)-triphenyl-arsoniumiodid 
• 19100-94-8 1,6-Bis-triphenylarsoniohexandiiodid 
• 19100-91-5 6-hydroxyhexyl-triphenylphosphonium iodide 
• 19100-92-6 hexane-1,6-diylbis(triphenylphosphonium)iodide 
• 26306-01-4 6-iodo-1-(trimethylsilyloxy)hexane 
• 1633-78-9 6-mercapto-1-hexanol 
• 497924-21-7 10-{3-[bis(4-methoxyphenyl)phenylmethoxy]hexyl}-3-(6-hydroxyhexyl)-7,8-dimethyl-10H-benzo[g]pteridin-2,4-dione 
• 500567-76-0 5-(6-hydroxy-hexyloxy)-benzene-1,3-dicarbaldehyde 
• 178697-36-4 1-[(6-fluorohexyl)oxy]-4-nitrobenzene 
• 78435-31-1 p-(ω-hydroxyhexyloxy)acetanilide 
• 666174-10-3 meta-(6-hydroxy)hexyloxyacetanilide 
• 118619-11-7 6-(4-aminophenoxy)hexan-1-ol 
• 386706-05-4 6-(3-aminophenoxy)hexan-1-ol 
• 2499-95-8 n-hexyl acrylate 

Relevant articles and documents

Thermal Cycloreversion of 2,2-Dimethyl-6-(ω-hydroxyalkyl)-4H-1,3-dioxin-4-ones: Mono-, Di-, and Trimeric Macrocyclic β-Keto Lactones by Intramolecular Trapping of (ω-Hydroxy)acylketenes

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Straightforward Synthesis of Fluorinated Enals via Photocatalytic α-Perfluoroalkenylation of Aldehydes

(Per)fluorinated substances represent an important compound class with regard to drug design and material chemistry. We found a mild, operationally simple, and inexpensive photocatalytic perfluoroalkenylation reaction giving tetrasubstituted, highly electron-deficient enals straight from aldehydes. This one-step reaction tolerates various functional groups and can be applied to a wide range of substrates giving the products in yields of 52-84%.

Transition-Metal-Free Borylation of Alkyl Iodides via a Radical Mechanism

We describe an operationally simple transition-metal-free borylation of alkyl iodides. This method uses commercially available diboron reagents as the boron source and exhibits excellent functional group compatibility. Furthermore, a diverse range of prim

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.