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Pyrimidine, 2,4,6-trichloro-5-methoxy-, also known as 2,4,6-Trichloro-5-methoxypyrimidine, is a chemical compound with the molecular formula C6H3Cl3N2O. It is a derivative of the pyrimidine ring structure, featuring three chlorine atoms and one methoxy group attached to the ring. Pyrimidine, 2,4,6-trichloro-5-methoxyis utilized in various chemical and pharmaceutical applications, serving as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is employed in research and development for the creation of new compounds with potential biological activities. Due to its potentially hazardous nature, it necessitates proper handling and storage with appropriate safety measures.

60703-46-0

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60703-46-0 Usage

Uses

Used in Pharmaceutical Industry:
Pyrimidine, 2,4,6-trichloro-5-methoxyis used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Pyrimidine, 2,4,6-trichloro-5-methoxyis utilized as an intermediate in the production of agrochemicals, aiding in the development of compounds with pesticidal or herbicidal properties.
Used in Research and Development:
Pyrimidine, 2,4,6-trichloro-5-methoxyis employed as a building block in research and development for the creation of new compounds with potential biological activities, contributing to the discovery of novel therapeutic agents or chemical entities with specific applications.
Safety Precautions:
Due to the potentially hazardous nature of Pyrimidine, 2,4,6-trichloro-5-methoxy-, it is crucial to handle and store Pyrimidine, 2,4,6-trichloro-5-methoxy- with proper safety measures to prevent any adverse effects on health or the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 60703-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,0 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60703-46:
(7*6)+(6*0)+(5*7)+(4*0)+(3*3)+(2*4)+(1*6)=100
100 % 10 = 0
So 60703-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3Cl3N2O/c1-11-2-3(6)9-5(8)10-4(2)7/h1H3

60703-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-Trichloro-5-methoxypyrimidine

1.2 Other means of identification

Product number -
Other names Pyrimidine,2,4,6-trichloro-5-methoxy

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:60703-46-0 SDS

60703-46-0Downstream Products

60703-46-0Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF

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Paragraph 0199, (2021/12/28)

The present disclosure relates to inhibitors of one or more isoforms of RAS, such as inhibitors of one or more of KRAS, HRAS and NRAS, or mutants thereof, such as G12D, G12V, G13D or G12C mutants thereof. Therapeutic methods of treating conditions and dis

Synthesis method of 2,4,6,-trichloro-5-methoxypyrimidine

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Paragraph 0014-0017, (2019/10/15)

The invention discloses a synthesis method of 2,4,6,-trichloro-5-methoxypyrimidine, the synthesis method comprises the following steps of: 1, mixing 2,4,6-trihydroxy-5-methoxypyrimidine, phosphorus oxychloride and an organic base according to a weight ratio of 1: 5-10: 0.33-0.7, and performing chlorination reaction at 25-100 DEG C for 2-5 hours; and 2, after the reaction is completed, cooling a mixture, concentrating the mixture under a reduced pressure to remove excess phosphorus oxychloride, quenching with water, extracting with an organic solvent, drying, and concentrating to obtain a product. The method not only improves the yield, shortens the time, is simple to operate, simplifies the post-treatment process, saves the cost, and is suitable for popularization.

DIOXINO-AND OXAZIN-[2,3-D]PYRIMIDINE PI3K INHIBITOR COMPOUNDS AND METHODS OF USE

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Page/Page column 0175, (2014/03/25)

Dioxino-and oxazin-[2,3-d]pyrimidine PI3K inhibitor compounds of Formula I with anti-cancer activity, anti-in-flammatory activity, or immunoregulatory properties, and more specifically with PI3 kinase modulating or inhibitory activity are de-scribed. Methods are described for using the tricyclic PI3K inhibitor compounds of Formula I for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, organisms, or associated pathological conditions.

TRICYCLIC PI3K INHIBITOR COMPOUNDS AND METHODS OF USE

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Page/Page column 84, (2012/06/30)

Tricyclic PI3k inhibitor compounds of Formula I with anti-cancer activity, anti- inflammatory activity, or immunoregulatory properties, and more specifically with PI3 kinase modulating or inhibitory activity are described. Methods are described for using the tricyclic PI3K inhibitor compounds of Formula I for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, organisms, or associated pathological conditions. Formula I compounds include stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof. The dashed lines indicate an optional double bond, and at least one dashed line is a double bond. The substituents are as described.

NOVEL PYRIMIDINE COMPOUNDS AS MTOR AND P13K INHIBITORS

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Page/Page column 217-218, (2011/07/30)

The present invention relates to pyrimidine compounds of formula (I): which are useful in treating mTOR kinase- or PI3K kinase-related diseases.

Pyrimidines

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, (2008/06/13)

Compounds having the formula SPC1 Process for the preparation of such compounds which comprises reacting a pound having the formula: SPC2 Medicaments containing a compound of formula (I) or a salt thereof with a pharmaceutically acceptable acid; compounds

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