4811-16-9

Basic information

• Product Name: 6-Hydroxymethyl-2-methyl-pyridin-3-ol
• Synonyms: 5-hydroxy-6-Methyl-2-PyridineMethanol;3-Hydroxy-6-hydroxymethyl-2-methylpyridine
• CAS NO: 4811-16-9
• Molecular Formula: C7H9NO2
• Molecular Weight: 139.15186
• Mol File: 4811-16-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 380.1 °C at 760 mmHg
• Flash Point: 183.6 °C
• Appearance: /
• Density: 1.251 g/cm³
• Vapor Pressure: 1.87E-06mmHg at 25°C
• Refractive Index: 1.589
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 6-Hydroxymethyl-2-methyl-pyridin-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Hydroxymethyl-2-methyl-pyridin-3-ol(4811-16-9)
• EPA Substance Registry System: 6-Hydroxymethyl-2-methyl-pyridin-3-ol(4811-16-9)

Safety Data

• Hazardous Substances Data: 4811-16-9(Hazardous Substances Data)

Usage

General Description

6-Hydroxymethyl-2-methyl-pyridin-3-ol, also known as vitamin B6, is a water-soluble vitamin that plays a crucial role in numerous biochemical reactions in the body. It is involved in the metabolism of amino acids, carbohydrates, and lipids, as well as in the synthesis of neurotransmitters and hemoglobin. This chemical is essential for the proper functioning of the nervous system, immune system, and overall health. Deficiency of vitamin B6 can lead to symptoms such as anemia, dermatitis, and neurological disorders. It is commonly found in a variety of foods, including meat, fish, whole grains, and vegetables, and is also available as a dietary supplement.

InChI:InChI=1/C7H9NO2/c1-5-7(10)3-2-6(4-9)8-5/h2-3,9-10H,4H2,1H3

Upstream product

• 1121-25-1 2-methyl-3-pyridinol 
• 50-00-0 formaldehyd 
• 7440-44-0 pyrographite 

Relevant articles and documents

Evidence for Reagent-Induced Spin-State Switching in Tripodal Fe(II) Iminopyridine Complexes

We present evidence of a spin-state change that accompanies desilylation reactions performed on two related Fe(II) iminopyridine coordination complexes. To probe these systems, we performed titrations with CsF in solution and analyzed the speciation with in situ magnetometry, electrochemistry, and mass spectrometry techniques. We find that pendant tert-butyldimethylsilyl groups are readily cleaved under these conditions, and the resulting desilylated complexes exhibit overall decreased solution magnetic susceptibility values. Density functional theory and ab initio computations probe the impact of substituent identity (prior to- and post-desilylation) on the metal-ligand σ-donor and -acceptor bonding properties. We attribute the observed spin-state changes to the decrease in entropy associated with the conformational freedom of the silylated high-spin complex, resulting in a more favored low-spin state upon desilylation.

SUBSTITUTED PYRIDINE AND PYRIMIDINE DERIVATIVES AND THEIR USE IN TREATING VIRAL INFECTIONS

The present invention provides compounds of Formula (I): and tautomers, isomers, and esters of said compounds, and pharmaceutically acceptable salts, solvates, and prodrugs of said compounds, wherein wherein each of R, R1, X, Y, Z, R2, R3, R4, R5, R6, R7, R8, R9, R18, R19 and n is selected independently and as defined herein. Compositions comprising such compounds are also provided. The compounds of the invention are effective as inhibitors of HCV, and are useful, alone and together with other therapeutic agents, in treating or preventing diseases or disorders such as viral infections and virus-related disorders.

alpha-AMINO METHYL-5-HYDROXY-2-PYRIDINEMETHANOLS

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