콘텐츠로 건너뛰기
Merck
모든 사진(1)

Key Documents

469920

Sigma-Aldrich

2-Ethynylpyridine

98%

동의어(들):

2-Pyridinylethyne, 2-Pyridylacetylene, Pyridin-2-ylacetylene

로그인조직 및 계약 가격 보기


About This Item

실험식(Hill 표기법):
C7H5N
CAS Number:
Molecular Weight:
103.12
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

refractive index

n20/D 1.56 (lit.)

bp

85 °C/12 mmHg (lit.)

density

1.021 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

C#Cc1ccccn1

InChI

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

InChI key

NHUBNHMFXQNNMV-UHFFFAOYSA-N

일반 설명

2-Ethynylpyridine is a pyridine derivative.

애플리케이션

2-Ethynylpyridine has been used to synthesize:
  • poly(2-ethynyl-N-iodopyridinium iodide), via in-situ uncatalyzed polymerization
  • poly[2-ethynyl-N-(2-furoyl)pyridinium chloride
  • poly[2-ethynyl-N-(propylsulfonate)pyridinium betaine]
  • 4-(2′-pyridyl)-1,2,3-triphospholide anion, via reaction with anionic heptaphosphide clusters
  • poly[N-(carboxymethyl)-2-ethynylpyridinium bromide], a new water-soluble ionic conjugated polymer
  • self-doped ionic conjugated polymer, poly(2-ethynylpyridinimum N-benzoylsulfonate).

기타 정보

It may darken in storage with no loss in purity.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number

적합한 버전을 찾을 수 없으신가요?

특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Yeong-Soon Gal et al.
Journal of nanoscience and nanotechnology, 14(8), 6247-6250 (2015-05-06)
A new ionic polyacetylene derivative with furoyl substituents was prepared by the uncatalyzed polymerization of 2-ethynylpyridine by using 2-furoyl chloride in high yield. The polymer structure was characterized by such instrumental methods as NMR, IR, and UV-visible spectroscopies to have
Cecilia Zavala-Tecuapetla et al.
Pharmacological reports : PR, 66(5), 927-930 (2014-08-26)
Action of an antagonist of metabotropic glutamate receptors subtype 5 MTEP was studied in a model of complex partial seizures. Dorsal hippocampus of rat pups 12, 18 and 25 days old was stimulated six times with 10-min intervals. MTEP (20
Robert S P Turbervill et al.
Inorganic chemistry, 52(9), 5527-5534 (2013-04-24)
Reactions between anionic heptaphosphide clusters ([P7](3-)/[HP7](2-)) and 2-ethynylpyridine yielded the 4-(2'-pyridyl)-1,2,3-triphospholide anion ([P3C2H(2-C5H4N)](-); 1). This species was isolated as a compositionally pure [K(2,2,2-crypt)](+) salt in moderate yields. Preliminary coordination studies of 1 toward Mo(CO)6 or Mo(py)3(CO)3 (py = pyridine) afforded
Yeong-Soon Gal et al.
Journal of nanoscience and nanotechnology, 12(5), 4361-4364 (2012-08-03)
A new water-soluble ionic conjugated polymer, poly[N-(carboxymethyl)-2-ethynylpyridinium bromide], was prepared by the activated polymerization of 2-ethynylpyridine by using bromoacetic acid. This polymerization proceeded well in mild reaction conditions without any additional initiator or catalyst. The polymer structure was characterized by
Yeong-Soon Gal et al.
Journal of nanoscience and nanotechnology, 14(10), 8028-8032 (2015-05-07)
Poly(2-ethynyl-N-iodopyridinium iodide) [PEIPI] was easily prepared via in-situ uncatalyzed polymerization of 2-ethynylpyridine by using iodine. The activated acetylenic bond of 2-ethynyl-N-iodopyridinium iodide formed at the initial reaction time was assumed to be susceptible to linear polymerization, followed by an identical

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

고객지원팀으로 연락바랍니다.