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251054

2-Hydroxypyridine-3-carboxylic acid

Name: 2-Hydroxypyridine-3-carboxylic acid
Brand: ALDRICH

98%

Synonym(s):

2-Hydroxynicotinic acid, 2-Hydroxypyridine-3-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):

C₆H₅NO₃

CAS Number:

609-71-2

Molecular Weight:

139.11

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24855099

EC Number:

210-198-2

Beilstein/REAXYS Number:

472167

MDL number:

MFCD00010100

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

258-261 °C (lit.)

solubility

formic acid: soluble 50 mg/mL, clear, colorless to yellow

functional group

carboxylic acid

SMILES string

OC(=O)c1cccnc1O

InChI

1S/C6H5NO3/c8-5-4(6(9)10)2-1-3-7-5/h1-3H,(H,7,8)(H,9,10)

InChI key

UEYQJQVBUVAELZ-UHFFFAOYSA-N

Description

Application

2-Hydroxypyridine-3-carboxylic acid may be used in chemical synthesis.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Synthesis and biological activity of 2-hydroxynicotinoyl-serine-butyl esters related to antibiotic UK-3A.

Ade Arsianti et al.

Bioorganic & medicinal chemistry letters, 20(14), 4018-4020 (2010-07-14)

Novel 2-hydroxynicotinoyl-serine-butyl esters have been synthesized. Three-step reactions from L-serine by esterification with n-butanol, amidation with 2-hydroxynicotinic acid and esterification with the corresponding carboxylic acids gave AD-1, AD-2 and AD-3. The toxicity level of esters were determined by Brine shrimp

Comparing the lipid membrane affinity and permeation of drug-like acids: the intriguing effects of cholesterol and charged lipids.

Anita V Thomae et al.

Pharmaceutical research, 24(8), 1457-1472 (2007-03-28)

Lipid bilayers regulate the passage of solutes into and between cellular compartments. A general prerequisite for this passage is the partitioning of the solute into the bilayer. We investigated the relationship between bilayer partitioning and permeation of three drug-like acids

Permeation of aromatic carboxylic acids across lipid bilayers: the pH-partition hypothesis revisited.