134079-02-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from cyclohexanedione, which is a six-membered ring with two carbonyl groups at the 1 and 3 positions. A bromophenyl methyl group is attached to the 2-position of the ring.
Explanation
The compound is used as a building block for the synthesis of various biologically active compounds, which can be further developed into pharmaceuticals.
Explanation
The compound has been studied for its potential to inhibit the growth of fungi and bacteria, which could be useful in the development of new anti-infective agents.
Explanation
The compound has been investigated for its ability to inhibit specific enzymes, which could be relevant in the development of drugs targeting enzyme-related diseases.
Explanation
The compound has been studied for its ability to form complexes with metal ions, which could be useful in various applications, such as catalysis or the development of new materials.
Explanation
The solubility of the compound in different solvents is not mentioned in the material provided. Solubility is an important property for determining the compound's reactivity and potential applications.
Explanation
The stability of the compound under various conditions (e.g., temperature, pH, etc.) is not mentioned in the material provided. Stability is an important factor to consider when evaluating the compound's suitability for specific applications.
Explanation
The reactivity of the compound with other chemicals or under different conditions is not mentioned in the material provided. Reactivity is a crucial property for understanding the compound's potential applications and limitations in chemical reactions.
Structure
Cyclohexanedione derivative with a bromophenyl methyl group at the 2-position
Application
Organic synthesis and pharmaceutical research
Biological and pharmacological activities
Anti-fungal and anti-bacterial properties
Enzyme inhibition
Potential use as an inhibitor for certain enzymes
Coordination chemistry
Potential use as a ligand for metal complexes
Solubility
Not specified in the provided material
Stability
Not specified in the provided material
Reactivity
Not specified in the provided material
Check Digit Verification of cas no
The CAS Registry Mumber 134079-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,0,7 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134079-02:
(8*1)+(7*3)+(6*4)+(5*0)+(4*7)+(3*9)+(2*0)+(1*2)=110
110 % 10 = 0
So 134079-02-0 is a valid CAS Registry Number.
134079-02-0Relevant academic research and scientific papers
Chiral Bronsted acid-promoted enantioselective desymmetrization in an intramolecular schmidt reaction of symmetric azido 1,3-hexanediones: Asymmetric synthesis of azaquaternary pyrroloazepine skeletons
Yang, Ming,Zhao, Yu-Ming,Zhang, Shu-Yu,Tu, Yong-Qiang,Zhang, Fu-Min
supporting information, p. 1344 - 1347 (2013/01/11)
The enantioselective desymmetrization of 2-substituted-2-azidopropyl 1,3-hexanediones through an asymmetric intramolecular Schmidt reaction using a chiral Bronsted acid has been developed for the first time. Synthetically interesting pyrroloazepine skeletons with an azaquaternary stereogenic center with up to 59 % ee are accessed effectively (see scheme; R=H, alkyl, or aryl). Copyright
One-pot reactions: Enantiomerically pure bicyclo[5.3.1]undecanes; Synthesis of a taxoid compound
Gutke, Hans-Jürgen,Braun, Norbert A.,Spitzner, Dietrich
, p. 8137 - 8141 (2007/10/03)
Reaction of C-2 substituted cyclohexenone with an enantiomerically pure α-bromopentenoate leads to enantiopure tricyclooctane, which can be transformed into a taxoid like compound having the typical bicyclo[5.3.1] undecane skeleton. Graphical Abstract
The Use of R3SiSnR'3 in Organic Synthesis. A Novel Palladium-Catalyzed Tandem Transmetalation-Cyclization Reaction
Mori, Miwako,Kaneta, Naotake,Shibasaki, Masakatsu
, p. 3486 - 3493 (2007/10/02)
The intramolecular coupling of vinyl triflates 12 with vinyl halides proceeded smoothly in the presence of Bu3SnSiMe3 (1a) and a palladium catalyst and gave cyclic products 13 via tandem intermolecular and intramolecular transmetalations.
