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2,6-dichloro-N-(2-Methoxyethyl)pyriMidin-4-aMine is a pyrimidine derivative with the molecular formula C8H10Cl2N4O. It features two chlorine atoms at the 2 and 6 positions of the pyrimidine ring and an N-(2-Methoxyethyl) group at the 4 position. This chemical compound serves as a building block in the synthesis of various pyrimidine-based compounds and holds potential for use in pharmaceuticals and agrochemicals due to its structural and pharmacological properties.
Used in Chemical Research:
2,6-dichloro-N-(2-Methoxyethyl)pyriMidin-4-aMine is used as a chemical intermediate for the synthesis of pyrimidine-based compounds, which are essential in various chemical reactions and processes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,6-dichloro-N-(2-Methoxyethyl)pyriMidin-4-aMine is used as a key component in the development of new drugs. Its unique structure and properties make it a valuable candidate for creating novel therapeutic agents.
Used in Agrochemical Research:
Similarly, in agrochemical research, 2,6-dichloro-N-(2-Methoxyethyl)pyriMidin-4-aMine is utilized as a starting material for the creation of new agrochemicals, potentially leading to advancements in crop protection and management.
It is crucial to handle 2,6-dichloro-N-(2-Methoxyethyl)pyriMidin-4-aMine with care and adhere to safety guidelines to mitigate any hazardous properties it may possess.

879609-73-1

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879609-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879609-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,6,0 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 879609-73:
(8*8)+(7*7)+(6*9)+(5*6)+(4*0)+(3*9)+(2*7)+(1*3)=241
241 % 10 = 1
So 879609-73-1 is a valid CAS Registry Number.

879609-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-N-(2-methoxyethyl)pyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 2,6-dichloro-N-(2-methoxyethyl)pyrimidin-4-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:879609-73-1 SDS

879609-73-1Relevant academic research and scientific papers

De novo design of nonpeptidic compounds targeting the interactions between interferon-α and its cognate cell surface receptor

Bello, Angelica M.,Bende, Tanushree,Wei, Lianhu,Wang, Xiaoyang,Majchrzak-Kita, Beata,Fish, Eleanor N.,Kotra, Lakshmi P.

, p. 2734 - 2743 (2008/12/22)

Type 1 interferons (IFN) bind specifically to the corresponding receptor, IFNAR. Agonists and antagonists for IFNAR have potential therapeutic value in the treatment of viral infections and systemic lupus erythematosus, respectively. Specific sequences on

Vanilloid receptor ligands and their use in treatments

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Page/Page column 71, (2010/10/20)

Substituted pyridines and pyrimidines and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

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