162238-27-9 Usage
Explanation
Different sources of media describe the Explanation of 162238-27-9 differently. You can refer to the following data:
1. The compound's full name, which includes its stereochemistry and classification in the Chemical Abstracts Service (CAS) registry.
2. The molecular formula representing the compound's composition, with 7 carbon (C), 9 hydrogen (H), 1 nitrogen (N), and 2 oxygen (O) atoms.
3. The compound is derived from 1,2-ethanediol, which is a common organic compound with various applications.
4. The compound has a pyridinyl group attached to it, which is a heterocyclic aromatic ring containing nitrogen.
5. The compound is classified as a heterocyclic compound due to the presence of a nitrogen atom in its ring structure.
6. The compound has potential applications in the fields of organic chemistry and pharmaceutical research, likely due to its unique structure and properties.
7. The compound may have hazardous properties, and it is essential to follow strict safety protocols when handling and using it.
8. The compound has a specific stereochemistry, with the (1S)-configuration indicating the arrangement of atoms in the molecule.
Derivative
1,2-Ethanediol (ethylene glycol)
Pyridinyl Group
Contains a pyridinyl group
Classification
Heterocyclic compound
Applications
Organic chemistry and pharmaceutical research
Safety Precautions
Handle with caution
Stereochemistry
(1S)-configuration
Check Digit Verification of cas no
The CAS Registry Mumber 162238-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,2,3 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162238-27:
(8*1)+(7*6)+(6*2)+(5*2)+(4*3)+(3*8)+(2*2)+(1*7)=119
119 % 10 = 9
So 162238-27-9 is a valid CAS Registry Number.
162238-27-9Relevant articles and documents
Microbiological transformations. Part 46: Preparation of enantiopure (S)-2-pyridyloxirane via epoxide hydrolase-catalysed kinetic resolution
Genzel, Yvonne,Archelas, Alain,Broxterman,Schulze, Birgit,Furstoss, Roland
, p. 3041 - 3044 (2000)
The hydrolytic kinetic resolution (HKR) of 2-pyridyloxirane is described, using the overexpressed epoxide hydrolase from the filamentous fungus Aspergillus niger. This allows the preparation of the (S)-enantiomer of this product in enantiopure form (ee >9
