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Merck
CN

479969

Sigma-Aldrich

4-氨基-5-嘧啶甲腈

96%

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About This Item

经验公式(希尔记法):
C5H4N4
CAS号:
分子量:
120.11
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

96%

表单

solid

mp

251-255 °C (lit.)

官能团

nitrile

SMILES字符串

Nc1ncncc1C#N

InChI

1S/C5H4N4/c6-1-4-2-8-3-9-5(4)7/h2-3H,(H2,7,8,9)

InChI key

JAIYUIOGVNRXEW-UHFFFAOYSA-N

一般描述

4-Amino-5-pyrimidinecarbonitrile (APC) is a pyrimidine derivative that has been synthesized via three-component reaction between benzaldehyde, benzamidine hydrochloride and malononitrile. The infrared, 1H NMR, 13C NMR and mass spectra of APC have been recorded.

应用

4-Amino-5-pyrimidinecarbonitrile may be used as a monodentate ligand to prepare metal complexes of Co(II), Ni(II), Cu(II) and Pd(II) ions. It may be used as a reactant to prepare 1H-pyrimido[4,5-d]pyrimidine-2,4-dione.

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Synthesis, antimicrobial activity, structural and spectral characterization and DFT calculations of Co (II), Ni (II), Cu (II) and Pd (II) complexes of 4-amino-5-pyrimidinecarbonitrile.
Mohamed TA, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 135, 417-427 (2015)
Infrared and NMR spectra, tautomerism, vibrational assignment, normal coordinate analysis, and quantum mechanical calculations of 4-amino-5-pyrimidinecarbonitrile.
Afifi MS, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 111, 277-289 (2013)
Three-component process for the synthesis of 4-amino-5-pyrimidinecarbonitriles under thermal aqueous conditions or microwave irradiation.
Sheibani H, et al.
ARKIVOC (Gainesville, FL, United States), 2, 115-123 (2008)
Synthesis of quinazoline-2,4(1H,3H)-diones from carbon dioxide and 2-aminobenzonitriles using [Bmim]OH as a homogeneous recyclable catalyst.
Patil YP, et al.
Catalysis Today, 148(3), 355-360 (2009)

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