1445-98-3

Basic information

• Product Name: Cyclohexane, 1-chloro-1-ethyl-
• CAS NO: 1445-98-3
• Molecular Formula: C8H15Cl
• Molecular Weight: 146.66
• Mol File: 1445-98-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 1-chloro-1-ethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1-chloro-1-ethyl-(1445-98-3)
• EPA Substance Registry System: Cyclohexane, 1-chloro-1-ethyl-(1445-98-3)

Safety Data

• Hazardous Substances Data: 1445-98-3(Hazardous Substances Data)

Usage

General Description

Cyclohexane, 1-chloro-1-ethyl- is a chemical compound with the molecular formula C8H15Cl. It is a chloroalkane derivative of cyclohexane, where a chlorine atom is attached to a carbon atom that is also bonded to an ethyl group. Cyclohexane, 1-chloro-1-ethyl- is commonly used as a solvent in various chemical reactions and processes due to its non-polar nature and ability to dissolve a wide range of substances. It is also utilized in the manufacturing of pharmaceuticals, pesticides, and other industrial chemicals. However, it is important to handle this chemical with caution as it is toxic and can cause irritation to the skin, eyes, and respiratory system upon exposure.

Upstream product

• 1003-64-1 ethylidenecyclohexane 
• 108-94-1 cyclohexanone 
• 507-20-0 tertiary butyl chloride 
• 1678-91-7 ethyl-cyclohexane 
• 1940-18-7 1-ethylcyclohexanol 

Downstream Products

• 1940-17-6 4-(1-ethyl-cyclohexyl)-phenol 
• 21504-65-4 1-ethyl-1-(2-chloro-ethyl)-cyclohexane 
• 1453-24-3 1-ethylcyclohexene 
• 1940-18-7 1-ethylcyclohexanol 
• 4926-90-3 1-methyl-1-ethylcyclohexane 
• 4926-93-6 1-butyl-1-ethylcyclohexane 
• 78-01-3 2,2-diethylcyclohexane 

Relevant articles and documents

Silica gel-mediated hydrohalogenation of unactivated alkenes using hydrohalogenic acids under organic solvent-free conditions

Silica gel-mediated hydrochlorination of unactivated alkenes using 35% hydrochloric acid under organic solvent-free conditions proceeded to give the corresponding chlorides in good yields. Hydrobromination or hydriodination using 47% hydrobromic acid or 55% hydriodic acid afforded the corresponding halides, respectively. Silica gel could be recycled five times without any significant loss of activities.

Preparation of ionic liquid-based vilsmier reagent from novel multi-purpose dimethyl formamide-like ionic liquid and its application

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Geminale Dialkylierung von Ketonen mit Grignard-Verbindungen und Methyltitan(IV)-chloriden

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