1119-67-1

Basic information

• Product Name: 1-Iodo-1-hexyne
• Synonyms: 1-Iodo-1-hexyne
• CAS NO: 1119-67-1
• Molecular Formula: C₆H₉I
• Molecular Weight: 208.04013
• Mol File: 1119-67-1.mol
• Article Data: 33

Chemical Properties

• Flash Point: 67℃
• Appearance: /
• Density: 1.564 at 20 °C
• Storage Temp.: 2-8°C
• BRN: 1740148
• CAS DataBase Reference: 1-Iodo-1-hexyne(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Iodo-1-hexyne(1119-67-1)
• EPA Substance Registry System: 1-Iodo-1-hexyne(1119-67-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/38
• Safety Statements: 26
• RIDADR: NA 1993 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 1119-67-1(Hazardous Substances Data)

Usage

Haloalkyne

A class of organic compounds containing both a halogen group (iodine in this case) and a triple bond between carbon atoms This defines the structure and functional groups present in 1-Iodo-1-hexyne.

Commonly used in organic synthesis

1-Iodo-1-hexyne serves as a building block for creating more complex molecules This highlights its role in the synthesis of other compounds.

Versatile reagent

Due to its unique structure, 1-Iodo-1-hexyne can participate in a variety of chemical reactions This emphasizes its usefulness in different chemical processes.

Potential applications in materials science and pharmaceutical research

1-Iodo-1-hexyne has been studied for its possible uses in these fields, indicating its potential for further development and application.

Hazardous to health and environment

Proper handling and storage of 1-Iodo-1-hexyne is crucial, as it can pose risks to both human health and the environment This serves as a warning for those working with the compound.

Upstream product

• 105205-72-9 C₁₅H₃₃BO 
• 693-02-7 hex-1-yne 
• 32359-01-6 hexenylmagnesium bromide 
• 60-29-7 diethyl ether 
• 7553-56-2 iodine 
• 7664-41-7 ammonia 
• 932-88-7 1-iodo-2-phenylethyne 
• 121826-88-8 C₉H₁₈B^(1-)*Li⁽¹⁺⁾ 

Downstream Products

• 36967-65-4 2-[1-Iodo-meth-(Z)-ylidene]-hexanoic acid cyclohexylamide 
• 99315-17-0 S-cyclohexyl hexanethioate 
• 594-04-7 dichloroiodomethane 
• 74966-64-6 1,2-Diodo-1-hexene 
• 693-02-7 hex-1-yne 
• 2432-79-3 S-butyl hexanethioate 
• 99332-99-7 n-Hexylthiohexanoat 
• 626-62-0 Cyclohexyl iodide 
• 130647-12-0 3-(1-hexynyl)-2-cyclohexen-1-one 
• 15325-54-9 (Z)-hex-1-en-1-ylbenzene 
• 141236-32-0 1-(methoxycarbonyl)-1-(phenylsulfonyl)-2-methylenecyclopentane 
• 138770-04-4 1-Benzenesulfonyl-2-hept-2-yn-(E)-ylidene-cyclopentanecarboxylic acid methyl ester 
• 134486-55-8 1-Phenyl-undec-6-yn-1-ol 
• 39546-87-7 (E)-2,3-dimethyl-4-nonene 

Relevant articles and documents

An easy preparation of iodoacetylenes

Reaction of terminal acetylenes with bis(sym-collidine)iodine(I) hexafluorophosphate in methylene chloride leads in good yields to the formation of iodoacetylenes.

Pd(0)-catalyzed iodoalkynation of norbornene scaffolds: The remarkable solvent effect on reaction pathway

A palladium-catalyzed iodoalkynation of norbornene has been realized with the use of alkynyl iodides 1, which is found to be strongly solventdependent. MeCN favors 1,7-iodoalkylation product 3 while CCl4 leads to 1,2-iodoalkylation product 4.

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Unsymmetrically substituted aliphatic diacetylenes

A general method for the synthesis of pure samples of unsymmetrically disubstituted diacetylenes of the type CH3-(CH2)(n)-C=C=C=C-CH2-OH (n=2,3,4,5) is described in detail. The materials could be polymerized thermally, in the liquid state.

COMPOUNDS, COMPOSITIONS, AND METHODS FOR MODULATING FERROPTOSIS AND TREATING EXCITOTOXIC DISORDERS

The present disclosure provides, inter alia, a compound having the structure (1). Also provided are compositions containing a pharmaceutically acceptable carrier and one or more compounds according to the present disclosure. Further provided are methods f

Annulation-Induced Cascade Transformation of 5-Iodo-1,2,3-triazoles to 2-(1-Aminoalkyl)benzoxazoles

Base-mediated cyclization of (5-iodo-1,2,3-triazolyl)phenols was proposed as a new synthetic strategy for the in situ generation of diazoimines via electrocyclic ring opening of the fused heterocycle. Cu-catalyzed amination of the intermediate diazoalkanes was employed to develop an efficient cascade approach to functionalized benzoxazoles.