Saltar al contenido
Merck
Todas las fotos(3)

Key Documents

View All Documentation

520446

Sigma-Aldrich

3-Ethynylpyridine

98%

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(3)

About This Item

Fórmula empírica (notación de Hill):
C7H5N
Número de CAS:
2510-23-8
Peso molecular:
103.12
MDL number:
MFCD02177459
UNSPSC Code:
12352100
PubChem Substance ID:
24874135
NACRES:
NA.22

assay

98%

bp

83-84 °C/30 mmHg (lit.)

mp

39-40 °C (lit.)

SMILES string

C#Cc1cccnc1

InChI

1S/C7H5N/c1-2-7-4-3-5-8-6-7/h1,3-6H

InChI key

CLRPXACRDTXENY-UHFFFAOYSA-N

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 3

flash_point_f

134.0 °F - closed cup

flash_point_c

56.67 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
MKCL6252
MKBZ1918V
MKBP5147V
MKBK3532V
MKBD7271

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

Busque por un COA

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Varinder K Aggarwal et al.
The Journal of organic chemistry, 68(13), 5381-5383 (2003-06-21)
A convenient one-pot procedure for the preparation of pyrazoles by 1,3-dipolar cycloaddition of diazo compounds generated in situ has been developed. Diazo compounds derived from aldehydes were reacted with terminal alkynes to furnish regioselectively 3,5-disubstituted pyrazoles. Furthermore, the reaction of
Wei Wei et al.
Chemical communications (Cambridge, England), 48(2), 305-307 (2011-11-18)
The first transition-metal-catalyzed direct oxidative synthesis of amides by using dioxygen as an oxygen source has been developed under mild conditions, in which DBU was used as the key additive. The present methodology, which utilizes dioxygen as an oxidant and
Christoph Gütz et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(33), 10890-10894 (2013-07-05)
A 1,1'-binaphthyl-based bis(pyridine) ligand (1) was prepared in racemic and enantiomerically pure form to study the formation of [Pd2(1)4] complexes upon coordination to palladium(II) ions with regard to the degree of chiral self-sorting. The self-assembly process proceeds in a highly
Qing Li et al.
Marine drugs, 16(4) (2018-03-31)
Chitosan is an abundant and renewable polysaccharide, which exhibits attractive bioactivities and natural properties. Improvement such as chemical modification of chitosan is often performed for its potential of providing high bioactivity and good water solubility. A new class of chitosan
Johan R Johansson et al.
The Journal of organic chemistry, 76(7), 2355-2359 (2011-03-11)
An experimentally simple sequential one-pot RuAAC reaction, affording 1,5-disubstituted 1H-1,2,3-triazoles in good to excellent yields starting from an alkyl halide, sodium azide, and an alkyne, is reported. The organic azide is formed in situ by treating the primary alkyl halide
Ver todos los artículos relacionados

Artículos

New Aromatic Terminal Alkynes

The terminal alkyne functionality has a wide range of applications including most recently the synthesis of spiropyran substituted 2,3-dicyanopyrazines and (±)-asteriscanolide, as well as conversion to enamines using resin-bound 2° amines.

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico