Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos

216879

Sigma-Aldrich

6-Aminopyridine-3-carboxylic acid

97%

Sinônimo(s):

6-Aminonicotinic acid

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(1)

About This Item

Fórmula empírica (Notação de Hill):
C6H6N2O2
Número CAS:
3167-49-5
Peso molecular:
138.12
Beilstein:
115992
Número CE:
221-630-4
Número MDL:
MFCD00006326
Código UNSPSC:
12352100
ID de substância PubChem:
24852983
NACRES:
NA.22

Ensaio

97%

pf

>300 °C (lit.)

cadeia de caracteres SMILES

Nc1ccc(cn1)C(O)=O

InChI

1S/C6H6N2O2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H2,7,8)(H,9,10)

chave InChI

ZCIFWRHIEBXBOY-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Categorias relacionadas

Descrição geral

Electrosynthesis of 6-aminopyridine-3-carboxylic acid (6-aminonicotinic acid) by electrochemical reduction of 2-amino-5-bromo and 2-amino-5-chloropyridine in the presence of CO2 at silver electrode has been reported.

Aplicação

6-Aminopyridine-3-carboxylic acid (6-Aminonicotinic acid) was used in the preparation of resin-bound 2-aminoazine.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 3

1 of 3

6-Amino-3-pyridinecarbonitrile 97%

Sigma-Aldrich

637475

6-Amino-3-pyridinecarbonitrile

4-Amino-nicotinic acid ≥97.0% (HPLC)

Sigma-Aldrich

11585

4-Amino-nicotinic acid

2-(1H-Imidazol-2-yl)pyridine 97%

Sigma-Aldrich

739405

2-(1H-Imidazol-2-yl)pyridine

A three-component solid-phase synthesis of 3-aminoimidazo [1, 2-a] azines.
Blackburn C.
Tetrahedron Letters, 39(31), 5469-5472 (1998)
Raman Sharma et al.
Xenobiotica; the fate of foreign compounds in biological systems, 49(12), 1447-1457 (2019-02-13)
1. The absorption, metabolism, and excretion of a single oral 450-mg dose of [14C]-(S)-6-(3-cyclopentyl-2-(4-trifluoromethyl)-1H-imidazol-1-yl)propanamido)nicotinic acid (PF-04991532), a hepatoselective glucokinase activator, was investigated in humans. Mass balance was achieved with ∼94.6% of the administered dose recovered in urine and feces. The
D J Jamieson et al.
Journal of bacteriology, 168(1), 389-397 (1986-10-01)
Expression of the tripeptide permease gene tppB is anaerobically induced. This induction is independent of the fnr (oxrA) gene product, which is known to be required for the anaerobic induction of several respiratory enzymes. We isolated, characterized, and mapped mutations
J W Foster et al.
Journal of general microbiology, 130(11), 2873-2881 (1984-11-01)
Mutants of Salmonella typhimurium supersensitive to the nicotinic acid analogue 6-amino-nicotinic acid (6ANA) were isolated as unable to grow on what are normally subinhibitory concentrations of the analogue. The mutations were classified on the basis of their map positions as
Electrocatalytic synthesis of 6-aminonicotinic acid at silver cathodes under mild conditions.
Gennaro A, et al.
Electrochemical Communications, 6(7), 627-631 (2004)

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica