CAS:40759-64-6
Molecular Formula:C18H20NiO2
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Nickel, [(1,2,5,6-η)-1,5-Cyclooctadiene][(2,3,5,6-η)-2,3,5,6-Tetramethyl-2,5-Cyclohexadiene-1,4-Dione]-; C10H12O2NiC8H12-1,5-Cyclo
Brief Introduction
Homogeneous catalyst
CAS:150529-93-4
Molecular Formula:C21H22N2O2
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(R,R)-2,2'-Bis(4-Phenyl-2-Oxazolin-2-yl)Propane; (R,R)-2,2'-(Dimethylmethylene)BIS(4-Phenyl-2-Oxazoline); (+)-2,2′-Isopropylidenebis[(4R)-4-Phenyl-2-Oxazoline]; (+)-2,2'-Isopropylidenebis[(4R)-4-Phenyl-2-Oxazoline]; (R,R)-2,2-Bis(4-Phenyl-2-Oxazolin-2-yl)Propane; (R,R)-2,2'-Isopropylidenebis(4-Phenyl-2-Oxazoline)
Brief Introduction
A nitrogen and oxygen containing ligand
CAS:9031-72-5
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NAD-Specific Aromatic Alcohol Dehydrogenases; Ethanol Oxidoreductases; 3-Methyl-2-Buten-1-ol Dehydrogenase; Alcohol Dehydrogenase 2; 3-Methyl-2-Buten-1-ol Dehydrogenases; NAD-Alcohol Dehydrogenase; ADH (Enzyme); Phenylethanol Dehydrogenase; Dehydrogenase, Alcohol (9CI); NADH-Alcohol Dehydrogenase; NADH-Aldehyde Reductase; NADH-Aldehyde Reductases; EC 1.1.1.1; NAD-Dependent alc. Dehydrogenases; E.C. 1.1.1.1; NAD-Specific Aromatic Alcohol Dehydrogenase; NAD-Dependent Alcohol Dehydrogenase; Ethanol Dehydrogenases; Alcohol Dehydrogenase (NAD); Acetaldehyde Reductases; Aliphatic Alcohol Dehydrogenases; Primary Alcohol Dehydrogenases; 14: PN: US20180023088 Seqid: 31 Claimed Protein; Ethanol Oxidoreductase; ADH; ADH (Enzymes); NADH-Alcohol Dehydrogenases; Acetaldehyde Reductase; Alcohol Dehydrogenases; Aliphatic Alcohol Dehydrogenase; NAD-Dependent Alcohol Dehydrogenases; Phenylethanol Dehydrogenases; Primary Alcohol Dehydrogenase; Ethanol Dehydrogenase; NAD-Dependent alc. Dehydrogenase
Brief Introduction
Alcohol dehydrogenase (ADH) is a zinc containing enzyme, which has high organ specificity in the body and is the most abundant in the liver. In normal physiological metabolism, ADH can catalyze the metabolism of ethanol (alcohol).
CAS:16057-43-5
Molecular Formula:C22H46O3
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Diethylene Glycol Monooctadecyl Ether; 2-(2-n-Octadecyloxyethoxy)Ethanol; 2-(2-Octadecyloxyethoxy)Ethanol; Diethylene Glycol Octadecyl Ether; 3,6-Dioxatetracosan-1-ol; Ethanol,2-[2-(Octadecyloxy)Ethoxy]; Diethylene Glycol Stearyl Ether; Steareth-2; Lipocol S-2; Steareth2
Brief Introduction
Stearyl alcohol polyether-2 is used as surfactant and emulsifier in cosmetics. It should be noted that excessive addition of this component will cause acne, allergy and other risks.
Brief Introduction
Total acetyl sugar generally refers to sugar derivatives in which all free hydroxyl (- OH) or amino (- NH2) in sugar molecules are protected by acetyl (- AC). Such molecules are an important synthetic intermediate in organic synthesis.
Total acetyl sugar refers to sugar derivatives in which all free hydroxyl (- OH) or amino (- NH2) in sugar molecules are protected by acetyl (- AC). For example, 1,2,3,4,6-o-pentaacetyl-d-glucopyranose (galactose, mannose) is common in the laboratory. It is widely used in many fields, such as sugar biology, sugar chemistry, synthetic chemistry, pharmaceutical chemistry, material science, physical chemistry and so on. For example, diacetyl glucose is a potential surfactant; In the synthesis of sugar molecules as raw materials, the preparation of total acetyl sugar is often the first step to protect the exposed hydroxyl groups, which is of great significance for the follow-up reaction.
Due to the wide application of total acetyl sugar in chemical experiments, the reagents such as total acetyl glucose, mannose and lactose prepared by the factory can be ordered directly on the market. However, for less experimental dosage, it is common to use the original sugar molecules to prepare acetyl sugar temporarily in the laboratory. At the same time, the total acetylation of monosaccharides such as glucose involves the preparation of chiral compounds, the application of thermodynamic and kinetic control theory, the influence of sugar end group effect on the product configuration, the influence of different catalysts on the product configuration ratio, as well as the basic experimental operations such as vacuum filtration, extraction and recrystallization. Therefore, learning to prepare total acetylsaccharides is of great significance for understanding the organic reaction mechanism and training the basic operations, It can be used as a good teaching content of College organic chemistry experiment course.
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