2611-00-9 Usage
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 known for its unique structure and reactivity. 3-Cyclohexenyl 3-cyclohexene 1-carboxylate serves as a versatile building block in the synthesis of various organic compounds, making it a valuable tool for organic chemists and researchers in the field of drug discovery and development.
Uses
Used in Pharmaceutical Industry:
3-Cyclohexenyl 3-cyclohexene 1-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Cyclohexenyl 3-cyclohexene 1-carboxylate is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Specialty Chemicals:
3-Cyclohexenyl 3-cyclohexene 1-carboxylate is employed as a building block in the synthesis of specialty chemicals, which are used in various industries for their unique properties and functions.
Used in Fragrance and Flavor Industry:
3-Cyclohexenyl 3-cyclohexene 1-carboxylate is also used in the production of fragrances and flavors, capitalizing on its reactivity and structural features to create novel and complex scents and tastes.
Overall, 3-Cyclohexenyl 3-cyclohexene 1-carboxylate has a wide range of applications in the chemical industry due to its versatile properties and uses, making it an essential component in the development of innovative products across multiple sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 2611-00-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2611-00:
(6*2)+(5*6)+(4*1)+(3*1)+(2*0)+(1*0)=49
49 % 10 = 9
So 2611-00-9 is a valid CAS Registry Number.
2611-00-9Relevant articles and documents
Rethinking the Claisen–Tishchenko Reaction
Morris, Stacey A.,Gusev, Dmitry G.
supporting information, p. 6228 - 6231 (2017/05/19)
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
Suzuki, Takeyuki,Matsuo, Tomohito,Watanabe, Kazuhiro,Katoh, Tadashi
, p. 1453 - 1455 (2007/10/03)
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
Ooi, Takashi,Ohmatsu, Kohsuke,Sasaki, Kouji,Miura, Tomoya,Maruoka, Keiji
, p. 3191 - 3193 (2007/10/03)
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.
