4806-74-0

Basic information

• Product Name: (1E)-2-chloro-N-hydroxycyclododecanimine
• Synonyms: 2-Chlorocyclododecanone oxime
• CAS NO: 4806-74-0
• Molecular Formula: C₁₂H₂₂ClNO
• Molecular Weight: 231.7622
• Mol File: 4806-74-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 359.752°C at 760 mmHg
• Flash Point: 171.372°C
• Density: 1.111g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.524
• CAS DataBase Reference: (1E)-2-chloro-N-hydroxycyclododecanimine(CAS DataBase Reference)
• NIST Chemistry Reference: (1E)-2-chloro-N-hydroxycyclododecanimine(4806-74-0)
• EPA Substance Registry System: (1E)-2-chloro-N-hydroxycyclododecanimine(4806-74-0)

Safety Data

• Hazardous Substances Data: 4806-74-0(Hazardous Substances Data)

Usage

General Description

(1E)-2-chloro-N-hydroxycyclododecanimine, also known as HC12, is a chemical compound with a molecular formula of C12H24ClNO. It is a hydroxylamine derivative, containing both a chloro and a hydroxyl group, and is derived from cyclododecane. HC12 has been studied for its potential use as an antibacterial and anti-biofilm agent, as well as for its role in catalyzing radical reactions. It has also been investigated for its ability to complex with transition metals and its potential application in organic synthesis. The compound's unique structure and properties make it a subject of interest for various research and development applications in the field of chemistry and pharmaceuticals.

Upstream product

• 1501-82-2 cyclododecene 

Relevant articles and documents

Oxidation of gem-chloronitroso- and vic-chloronitroso-alkanes and -cycloalkanes to respective chloronitro compounds by novel cetyltrimethylammonium hypochlorite reagent

Cetyltrimethylammonium hypochlorite (CTAHC) is prepared and used as an oxidizing agent for nitroso group to nitro group. The gem-chloronitroso and vic-chloronitroso compounds are prepared respectively from ketoximes and olefins by reacting with NOCl generated in situ from chlorotrimethylsilane (TMSC1 (l) and iso-amyl nitrite. CTAHC oxidizes gem-chloronitroso and vic-chloronitroso compounds to the corresponding chloronitro derivatives. While gem-chloronitro compounds are obtained in good yields, the vic-chloronitro derivatives are formed in moderate yields, because of the propensity of the vic-chloronitroso group to tautomerize to α-chlorooxime. The present method is simple and practical, particularly for the preparation of vic-chloronitro compounds, considering the fact that the known methods of their preparation are few and quite involved. Indian Academy of Sciences.