2611-00-9

Basic information

• Product Name: 3-Cyclohexenyl 3-cyclohexene 1-carboxylate
• Synonyms: 3-cyclohexene-1-carboxylic acid 3-cyclohexen-1-ylmethyl ester;3-Cyclohexenyl 3-cyclohexene 1-carboxylate;cyclohex-3-enylmethyl cyclohex-3-enecarboxylate;CYCLOHEX-3-EN-1-YLMETHYL CYCLOHEX-3-ENE-1-CARBOXYLATE;3-Cyclohexen-1-yl-methyl-3-cyclohexene-1-carboxylate;3-Cyclohexene-1-carboxylic acid (3-cyclohexenyl)methyl ester;3-Cyclohexene-1-carboxylic acid 3-cyclohexenylmethyl ester;cyclohex-3-ene-1-carboxylic acid cyclohex-3-en-1-ylmethyl ester
• CAS NO: 2611-00-9
• Molecular Formula: C₁₄H₂₀O₂
• Molecular Weight: 220.31
• EINECS: 220-031-5
• Product Categories: Fine Chemicals
• Mol File: 2611-00-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 303.8 °C at 760 mmHg
• Flash Point: 130.2 °C
• Appearance: /
• Density: 1.033 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-Cyclohexenyl 3-cyclohexene 1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Cyclohexenyl 3-cyclohexene 1-carboxylate(2611-00-9)
• EPA Substance Registry System: 3-Cyclohexenyl 3-cyclohexene 1-carboxylate(2611-00-9)

Safety Data

• Hazardous Substances Data: 2611-00-9(Hazardous Substances Data)

Usage

General Description

3-Cyclohexenyl 3-cyclohexene 1-carboxylate is a chemical compound with the molecular formula C14H20O2. It is categorized as a cyclohexene carboxylate and is typically used in the synthesis of other organic compounds. This chemical is often employed as a building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used in the production of fragrances and flavors. Its unique structure and reactivity make it a valuable tool for organic chemists and researchers in the field of drug discovery and development. Overall, 3-Cyclohexenyl 3-cyclohexene 1-carboxylate has a wide range of applications in the chemical industry due to its versatile properties and uses.

Upstream product

• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 72581-32-9 cyclohex-3-enylmethanol 

Downstream Products

• 2386-87-0 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate 

Relevant articles and documents

Rethinking the Claisen–Tishchenko Reaction

Pincer-type complexes [OsH2(CO){PyCH2NHCH2CH2NHPtBu2}] and [OsH2(CO){HN(CH2CH2PiPr2)2}] catalyze the disproportionation reaction of aldehydes via an outer-sphere bifunctional mechanism achieving turnover frequencies up to 14 000 h?1. The N?H group of the catalysts is a key player in this process, elucidated with the help of DFT calculations.

Iridium-catalyzed oxidative dimerization of primary alcohols to esters using 2-butanone as an oxidant

Oxidative dimerization of primary alcohols with 2-butanone in the presence of an amino alcohol-based Ir bifunctional catalyst was accomplished for the first time. The reaction proceeds with 1-2 mol% of the catalyst and 0.3 mol equivalents of K2CO3 in 2-butanone at room temperature to give the corresponding dimeric esters in 30-93% yield. Georg Thieme Verlag Stuttgart.

Isopropoxyaluminum 1,1′-biphenyl-2-oxy-2′-perfluorooctanesulfonamide as a catalyst for Tishchenko reaction

Isopropoxyaluminum 1,1′-biphenyl-2-oxy-2′-perfluorooctanesulfonamide (3) has been evaluated as an aluminum-based catalyst for the Tishchenko reaction. Compound 3 was found to exert high catalytic activity in the reaction with aliphatic aldehydes and also enabled smooth dimerization of enolizable aldehydes. This advantage was highlighted by the quantitative formation of ethyl acetate from acetaldehyde by the present system.