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1,2-Ethanediol,1-(2-pyridinyl)-,(1S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162238-27-9 Structure
  • Basic information

    1. Product Name: 1,2-Ethanediol,1-(2-pyridinyl)-,(1S)-(9CI)
    2. Synonyms: 1,2-Ethanediol,1-(2-pyridinyl)-,(1S)-(9CI)
    3. CAS NO:162238-27-9
    4. Molecular Formula: C7H9NO2
    5. Molecular Weight: 139.15
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 162238-27-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-Ethanediol,1-(2-pyridinyl)-,(1S)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Ethanediol,1-(2-pyridinyl)-,(1S)-(9CI)(162238-27-9)
    11. EPA Substance Registry System: 1,2-Ethanediol,1-(2-pyridinyl)-,(1S)-(9CI)(162238-27-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 162238-27-9(Hazardous Substances Data)

162238-27-9 Usage

Explanation

The compound's full name, which includes its stereochemistry and classification in the Chemical Abstracts Service (CAS) registry.

Explanation

The molecular formula representing the compound's composition, with 7 carbon (C), 9 hydrogen (H), 1 nitrogen (N), and 2 oxygen (O) atoms.

Explanation

The compound is derived from 1,2-ethanediol, which is a common organic compound with various applications.

Explanation

The compound has a pyridinyl group attached to it, which is a heterocyclic aromatic ring containing nitrogen.

Explanation

The compound is classified as a heterocyclic compound due to the presence of a nitrogen atom in its ring structure.

Explanation

The compound has potential applications in the fields of organic chemistry and pharmaceutical research, likely due to its unique structure and properties.

Explanation

The compound may have hazardous properties, and it is essential to follow strict safety protocols when handling and using it.

Explanation

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

Synthesis of Optically Active Hydroxyalkylpyridines and Related Pyridyl Amines

Chelucci, Giorgio,Cabras, M. Antonietta,Saba, Antonio

, p. 1973 - 1978 (2007/10/02)

2-(1-Hydroxyalkyl)pyridines have been prepared by cobalt(I)-catalyzed cocyclotrimerization reaction of O-protected α-hydroxynitriles with acetylene.From these compounds the related pyridyl amines have been obtained.

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