Search

  • Order Status
  • Quick Order
  • Promos
Element SearchElement SearchStructure SearchStructure Search
2-Chloro-6-hydroxypyridine, 98%
2-Chloro-6-hydroxypyridine, 98%
2-Chloro-6-hydroxypyridine, 98%
Thermo Scientific Chemicals

2-Chloro-6-hydroxypyridine, 98%

CAS: 16879-02-0 | C5H4ClNO | 129.543 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
100 g
ChemDexTry the chem dexTM web app
Catalog number A13164.14
also known as A13164-14
Price (EUR)
61,50
Each
Quantity:
25 g
Request bulk or custom format
Price (EUR)
61,50
Each
Chemical Identifiers
CAS16879-02-0
IUPAC Name6-chloro-1,2-dihydropyridin-2-one
Molecular FormulaC5H4ClNO
InChI KeyCLNNBQDAAGDAHI-UHFFFAOYSA-N
SMILESClC1=CC=CC(=O)N1
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale yellow
FormCrystals or powder or crystalline powder
Assay (Silylated GC)≥97.5%
Melting Point (clear melt)126.5-132.5?C
6-chloro-2-hydroxypyridine was used to study the synthesis, electrochemistry, spectroscopic properties and X-ray crystal structure of Os2Cl(chp)4 (chp = 6-chloro-2- hydroxypyridinate) complex. It undergoes melt reaction with Os2(O2CCH3)4CI2 at 145°C to yield Os2CI4(chp) and Os2Cl(chp)4.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
6-chloro-2-hydroxypyridine was used to study the synthesis, electrochemistry, spectroscopic properties and X-ray crystal structure of Os2Cl(chp)4 (chp = 6-chloro-2- hydroxypyridinate) complex. It undergoes melt reaction with Os2(O2CCH3)4CI2 at 145°C to yield Os2CI4(chp) and Os2Cl(chp)4.

Notes
Store at room temperature. Ensure adequate ventilation. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Daniel L. Comins.; Hao Hong.; Gao Jianhua. Asymmetric synthesis of camptothecin alkaloids: A nine-step synthesis of (S)-camptothecin. Tetrahedron Lett. 1994, 35 (30), 5331-5334 .
  2. Daniel L. Comins.; Jason M. Nolan. A Practical Six-Step Synthesis of (S)-Camptothecin.Org. Lett. 2001, 3 (26),4255-4257 .