159474-87-0 Usage
Explanation
The compound's full name, which includes its stereochemistry and classification.
Explanation
A more common and simplified name for the compound, which describes its structure.
Explanation
The compound belongs to the class of diols, which are organic compounds containing two hydroxyl (-OH) groups.
Explanation
The compound has a chiral center, which means it has a specific stereochemistry that can exist in different forms (enantiomers).
Explanation
The compound has a specific stereochemistry, denoted by the (1R) configuration, which describes the arrangement of atoms in three-dimensional space.
Explanation
The compound is used as a building block in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.
7. Metal-catalyzed cross-coupling reactions
Explanation
The compound is used in the production of metal-catalyzed cross-coupling reactions, which are essential for the synthesis of complex organic molecules.
Explanation
The compound has shown potential as a ligand in the coordination chemistry of transition metal complexes, which can lead to new applications in various fields.
Explanation
The compound has important applications in various fields of chemical research and industry, including the development of new drugs, agrochemicals, and other complex organic molecules.
Class
Diols
Chirality
Chiral compound
Stereochemistry
(1R) configuration
Applications
Organic synthesis, pharmaceuticals, agrochemicals
Coordination chemistry
Potential as a ligand in transition metal complexes
Fields of application
Chemical research and industry
Check Digit Verification of cas no
The CAS Registry Mumber 159474-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,7 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159474-87:
(8*1)+(7*5)+(6*9)+(5*4)+(4*7)+(3*4)+(2*8)+(1*7)=180
180 % 10 = 0
So 159474-87-0 is a valid CAS Registry Number.
159474-87-0Relevant articles and documents
New Chiral Modifiers for the Enantioselective Hydrogenation of Ethyl Pyruvate over Pt/Al2O3 Catalysts
Wang, Guozhi,Heinz, Thomas,Pfaltz, Andreas,Minder, Bruno,Mallat, Tamas,Baiker, Alfons
, p. 2047 - 2048 (1994)
Catalytic quantities of structurally simple chiral amino alcohols such as 2-(1-pyrrolidinyl)-1-(1-naphthyl)ethanol can induce enantioselectivities of up to 75percent e.e. in the hydrogenation of ethyl pyruvate over Pt/Al2O3 catalysts.
QUINOLONE ANTIBACTERIAL AGENTS
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Page/Page column 86; 111; 112, (2010/02/11)
Compounds of formula (I, II, III, IV, V, and VI) and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula (I) as well as pharmaceutically acceptable compositions comprising compounds of formula (I). Compounds of formula (I) as disclosed herein can be used in a variety of applications including use as antibacterial agents.
A new class of chiral modifiers for the enantioselective hydrogenation of α-ketoesters with Pt/Al2O3
Simons,Wang,Heinz,Giger,Mallat,Pfaltz,Baiker
, p. 505 - 518 (2007/10/02)
A series of enantiomerically pure chiral amino alcohols have been synthesized and applied as modifiers in the enantioselective hydrogenation of ethyl pyruvate over supported Pt catalysts. Their use enabled an enantiomeric excess of up to 75%. A molecular modelling study of the modifiers and reactant on a Pt(111) surface provides explanation for the observed enantiodifferentiation.
