159474-87-0

Basic information

• Product Name: 1,2-Ethanediol,1-(4-pyridinyl)-,(1R)-(9CI)
• Synonyms: 1,2-Ethanediol,1-(4-pyridinyl)-,(1R)-(9CI)
• CAS NO: 159474-87-0
• Molecular Formula: C₇H₉NO₂
• Molecular Weight: 139.15
• Product Categories: PYRIDINE
• Mol File: 159474-87-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 336.3±27.0 °C(Predicted)
• Appearance: /
• Density: 1.250±0.06 g/cm3(Predicted)
• PKA: 12.70±0.20(Predicted)
• CAS DataBase Reference: 1,2-Ethanediol,1-(4-pyridinyl)-,(1R)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Ethanediol,1-(4-pyridinyl)-,(1R)-(9CI)(159474-87-0)
• EPA Substance Registry System: 1,2-Ethanediol,1-(4-pyridinyl)-,(1R)-(9CI)(159474-87-0)

Safety Data

• Hazardous Substances Data: 159474-87-0(Hazardous Substances Data)

Usage

Explanation

Different sources of media describe the Explanation of 159474-87-0 differently. You can refer to the following data:
1. The compound's full name, which includes its stereochemistry and classification.
2. A more common and simplified name for the compound, which describes its structure.
3. The compound belongs to the class of diols, which are organic compounds containing two hydroxyl (-OH) groups.
4. The compound has a chiral center, which means it has a specific stereochemistry that can exist in different forms (enantiomers).
5. The compound has a specific stereochemistry, denoted by the (1R) configuration, which describes the arrangement of atoms in three-dimensional space.
6. 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
7. The compound is used in the production of metal-catalyzed cross-coupling reactions, which are essential for the synthesis of complex organic molecules.
8. 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.
9. 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

Upstream product

• 100-43-6 4-vinylpyridine 

Relevant articles and documents

New Chiral Modifiers for the Enantioselective Hydrogenation of Ethyl Pyruvate over Pt/Al2O3 Catalysts

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.

A new class of chiral modifiers for the enantioselective hydrogenation of α-ketoesters with Pt/Al2O3

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.