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Merck
모든 사진(3)

문서

193291

Sigma-Aldrich

2-Chloropyrimidine

95%

동의어(들):

2-Chloro-1,3-pyrimidine, Pyrimidin-2-yl chloride

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모든 사진(3)

About This Item

실험식(Hill 표기법):
C4H3ClN2
CAS Number:
1722-12-9
Molecular Weight:
114.53
Beilstein:
107171
EC Number:
217-020-2
MDL number:
MFCD00006060
UNSPSC 코드:
12352100
PubChem Substance ID:
24851590
NACRES:
NA.22

분석

95%

형태

crystals

bp

75-76 °C/10 mmHg (lit.)

mp

63-66 °C (lit.)

SMILES string

Clc1ncccn1

InChI

1S/C4H3ClN2/c5-4-6-2-1-3-7-4/h1-3H

InChI key

UNCQVRBWJWWJBF-UHFFFAOYSA-N

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관련 카테고리

일반 설명

2-Chloropyrimidine undergoes cobalt-catalyzed cross-coupling reaction with aryl halides.

애플리케이션

2-Chloropyrimidine was used in the synthesis of:
  • novel bis(2-(pyrimidin-2-yl)ethoxy)alkanes
  • 4′-(1,1′-(5-(2-methoxyphenoxy)-[2,2′-bipyrimidine]-4,6-diyl)bis(1H-pyrazol-3,1-diyl)) dianiline fluorescent dye, biosensor for protein assay
  • cis- and trans-octahydropyrrolo[2,3]pyridine derivatives
  • 2-amino-4-heteroarylpyrimidines

기타 정보

Remainder 2-hydroxypyrimidine

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

208.4 °F - closed cup

Flash Point (°C)

98 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

시험 성적서(COA)

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문서 라이브러리 방문

Vangavaragu Jhansi Rani et al.
Archiv der Pharmazie, 345(8), 663-669 (2012-05-18)
The pyrimidine nucleus is an important component of nucleic acids (DNA and RNA) and vitamins (B(2) and folic acid). It is evident from the literature that pyrimidine derivatives possess a wide spectrum of biological activities such as antioxidant, anticancer, antibacterial
Matthew G Bursavich et al.
Organic letters, 7(19), 4113-4116 (2005-09-09)
[reaction: see text] An expedient synthesis of diverse 2-amino-4-heteroarylpyrimidines via a 2-chloropyrimidine intermediate is described. A series of potentially biologically active analogues have been synthesized in two parallel steps to afford focused arrays.
Vikas S Padalkar et al.
Chemistry Central journal, 5, 72-72 (2011-11-10)
Fluorescent dyes with biocompatible functional group and good fluorescence behavior are used as biosensor for monitoring different biological processes as well as detection of protein assay. All reported fluorophore used as sensors are having high selectivity and sensitivity but till
Carina Sollert et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(14), 5380-5386 (2015-02-18)
The Ru-catalysed C2-H arylation of indoles and pyrroles by using boronic acids under oxidative conditions is reported. This reaction can be applied to tryptophan derivatives and tolerates a wide range of functional groups on both coupling partners, including bromides and
Igor Goljer et al.
Chirality, 21(7), 681-691 (2008-09-17)
Reaction of (S)- or (R)-3-aminoquinuclidine with 2-chloropyrimidine or 2-bromopyrimidine led to an unexpected formation of both cis- and trans-octahydropyrrolo [2,3]pyridine derivatives. A single-step synthesis of two of the four stereoisomers of these octahydropyrrolo[2,3]pyridine derivatives provides a convenient way of generating
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