6578-76-3 Usage
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in a molecule of 1,3-Dioxolane-4-methanol, 2-phenyl-, trans-.
Explanation
The compound is a colorless liquid at room temperature, which makes it suitable for use in various applications.
Explanation
Due to its ability to dissolve other substances, 1,3-Dioxolane-4-methanol, 2-phenyl-, transis often used as a solvent in various chemical processes.
Explanation
The compound is utilized in the production of various products, including fragrances, pharmaceuticals, and other organic compounds due to its unique properties.
Explanation
1,3-Dioxolane-4-methanol, 2-phenyl-, transserves as a starting material or building block in the synthesis of other chemical compounds.
Explanation
The transconfiguration refers to the arrangement of the phenyl and hydroxyl groups in the molecule, which influences its chemical and physical properties.
Explanation
The specific arrangement of the phenyl and hydroxyl groups in the transconfiguration affects the compound's reactivity, stability, and other physical properties.
Explanation
Due to its unique properties and the ability to act as a solvent, intermediate, and component in the production of various products, 1,3-Dioxolane-4-methanol, 2-phenyl-, transhas a broad range of applications across different industries.
Physical State
Colorless liquid
Solvent Properties
Commonly used as a solvent
Applications
Production of fragrances, pharmaceuticals, and other organic compounds
Intermediate in Synthesis
Used as an intermediate in the synthesis of other chemicals
Configuration
trans-
Chemical and Physical Properties
Determined by the transconfiguration
Versatility
Wide range of applications in various industries
Check Digit Verification of cas no
The CAS Registry Mumber 6578-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6578-76:
(6*6)+(5*5)+(4*7)+(3*8)+(2*7)+(1*6)=133
133 % 10 = 3
So 6578-76-3 is a valid CAS Registry Number.
6578-76-3Relevant academic research and scientific papers
The Chiral Target of Daptomycin Is the 2R,2′S Stereoisomer of Phosphatidylglycerol
Moreira, Ryan,Taylor, Scott D.
supporting information, (2021/12/09)
Daptomycin (dap) is an important antibiotic that interacts with the bacterial membrane lipid phosphatidylglycerol (PG) in a calcium-dependent manner. The enantiomer of dap (ent-dap) was synthesized and was found to be 85-fold less active than dap against
New synthesis of sn-1,2- and sn-2,3-O-diacylglycerols application to the synthesis of enantiopure phosphonates analogous to triglycerides: A new class of inhibitors of lipases
Marguet, Frank,Cavalier, Jean-Francois,Verger, Robert,Buono, Gerard
, p. 1671 - 1678 (2007/10/03)
Phosphonate compounds mimic the first transition state occurring during enzymatic carboxyester hydrolysis of natural substrates by forming a covalent bond with the catalytic serine. However, until now the organophosphorus compounds used in the inhibition studies more or less resembled a natural triglyceride substrate. In order to elucidate the interfacial activation and the mechanism of action of lipases, specific inhibitors need to be prepared. To achieve this goal, enantiomerically pure sn-1,2- and sn-2,3O- didecanoylglycerol compounds were prepared - starting from a C-4 chiral synthon, 3-buten-1,2-diol - and treated with n-pentylphosphonic dichloride and p-nitrophenol to afford the corresponding diastereomeric phosphonates, which were acylglycerol analogs. Subsequent separation of each of the phosphonate diastereomers A/B or ent-A/ent-B, performed by HPLC, led to four enantiopure stereoisomers that will be investigated as inhibitors of Human Pancreatic Lipase (HPL) and Human Gastric Lipase (HGL) using the monomolecular film technique.
