主要文件

查看所有文档

193291

2-氯嘧啶

Name: 2-氯嘧啶
Brand: ALDRICH

95%

别名:

2-氯-1,3-嘧啶, 嘧啶-2-酰氯

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₄H₃ClN₂

化学文摘社编号:

1722-12-9

分子量:

114.53

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851590

EC Number:

217-020-2

Beilstein/REAXYS Number:

107171

MDL number:

MFCD00006060

Assay:

95%

Form:

crystals

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

Quality Level

100

assay

95%

form

crystals

bp

75-76 °C/10 mmHg (lit.)

mp

63-66 °C (lit.)

functional group

chloro

SMILES string

Clc1ncccn1

InChI

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

InChI key

UNCQVRBWJWWJBF-UHFFFAOYSA-N

说明

General description

2-氯嘧啶可与芳基卤化物发生经钴催化的交叉偶联反应。

Application

2-氯嘧啶可用于合成：

新双（2-（嘧啶-2-基）乙氧基）烷烃
4′-（1,1′-（5-（2-甲氧基苯氧基）-[2,2′-联嘧啶基]-4,6-二基）双（1H-吡唑-3,1-二基））二苯胺荧光染料，可用作蛋白质测定的生物传感器
顺式-和反式-氢化吡咯并[2,3]吡啶衍生物
2-氨基-4-杂芳基嘧啶

Other Notes

残留物为 2-羟基嘧啶

pictograms

GHS07

signalword

Warning

hcodes

H302,H319

pcodes

P264 - P280 - P301 + P312 - P305 + P351 + P338 - P337 + P313 - P501

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

208.4 °F - closed cup

flash_point_c

98 °C - closed cup

ppe

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Synthesis and spectral characterization of new bis(2-(pyrimidin-2-yl)ethoxy)alkanes and their pharmacological activity.

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

Expedient parallel synthesis of 2-amino-4-heteroarylpyrimidines.

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.

Unexpected rearrangement of enantiomerically pure 3-aminoquinuclidine as a simple way of preparing diastereomeric octahydropyrrolo[2,3-c]pyridine derivatives.

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

查看所有相关文献

全球贸易项目编号

货号	GTIN
193291-10G	04061838760746
193291-50G	04061832241999