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4,5,6-trichloropyrimidin-2-amine is a chemical compound with the molecular formula C4HCl3N3, belonging to the pyrimidine family and featuring three chlorine atoms attached to the pyrimidine ring. It is recognized for its potent biological activity and reactivity, making it a valuable intermediate in the synthesis of a variety of pharmaceuticals, herbicides, and agrochemicals. However, it is also known for its potential environmental persistence and toxicity, necessitating careful regulation in its usage and disposal to mitigate adverse health and environmental effects.

51501-53-2

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51501-53-2 Usage

Uses

Used in Pharmaceutical Industry:
4,5,6-trichloropyrimidin-2-amine is used as a key intermediate in the synthesis of various pharmaceuticals due to its potent biological activity, contributing to the development of new drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4,5,6-trichloropyrimidin-2-amine is utilized as a building block for the production of herbicides and other crop protection agents, enhancing their effectiveness in controlling weeds and pests while ensuring crop yield and quality.
Used in Environmental Regulation:
4,5,6-trichloropyrimidin-2-amine is subject to careful usage and disposal guidelines to prevent its environmental persistence and toxicity. This involves the development and implementation of regulatory measures to minimize its negative impacts on health and the environment, ensuring sustainable chemical management practices.

Check Digit Verification of cas no

The CAS Registry Mumber 51501-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,0 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51501-53:
(7*5)+(6*1)+(5*5)+(4*0)+(3*1)+(2*5)+(1*3)=82
82 % 10 = 2
So 51501-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H2Cl3N3/c5-1-2(6)9-4(8)10-3(1)7/h(H2,8,9,10)

51501-53-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,6-Trichloropyrimidin-2-amine

1.2 Other means of identification

Product number -
Other names 4,5,6-Trichloro-pyrimidin-2-ylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51501-53-2 SDS

51501-53-2Downstream Products

51501-53-2Relevant academic research and scientific papers

PREPARATION AND USES OF PYRIMIDINONE DERIVATIVES

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Page/Page column 224-225, (2018/04/20)

The present invention relates to compounds of formula (I), and salts and solvates thereof, that function as inhibitors of cell division cycle 7 (Cdc7) kinase enzyme activity: (Formula (I)) wherein X, R1, R2, and n are each as defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as well as other diseases or conditions in which Cdc7 kinase activity is implicated.

PYRIMIDINONE DERIVATIVES AS CDC7 INHIBITORS

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Paragraph 00231-00232, (2018/05/27)

The present invention relates to compounds of formula I as defined herein, and salts and solvates thereof, that function as inhibitors of cell division cycle 7 (Cdc7) kinase enzyme activity Formula (I). The present invention also relates to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as well as other diseases or conditions in which Cdc7 kinase activity is implicated.

Syntheses of 2-amino-4,6-dichloro-5-nitropyrimidine and 2-amino-4,5,6-trichloropyrimidine: an unusual aromatic substitution

Lopez, Sergio,McCabe, Thomas,Stanley McElhinney,McMurry, T. Brian H.,Rozas, Isabel

supporting information; experimental part, p. 6022 - 6024 (2010/03/03)

2-Amino-4,6-dichloro-5-nitropyrimidine is an intermediate required for the preparation of nitropyrimidines as inactivators of the DNA repairing protein MGMT. When attempting its synthesis, 2-amino-4,5,6-trichloropyrimidine is obtained instead, via unusual aromatic substitution of the nitro group in 2-amino-4-hydroxy-5-nitropyrimidin-6-one by chloride. The synthesis, the reactivity of 4,5,6-trichloropyrimidine and the efficient preparation of 2-amino-4,6-dichloro-5-nitropyrimidine are presented.

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