701-78-0

Basic information

• Product Name: 2-AMINO-4-ETHYL-6-METHOXY-1,3,5-TRIAZINE
• Synonyms: 2-AMINO-4-ETHYL-6-METHOXY-1,3,5-TRIAZINE;5-triazin-2-amine,4-ethyl-6-methoxy-3;4-ethyl-6-methoxy-1,3,5-triazin-2-amine;2-AMINO-4-ETHYL-6-METHOXY-S-TRIAZINE;(4-ethyl-6-methoxy-s-triazin-2-yl)amine;1,3,5-Triazin-2-aMine, 4-ethyl-6-Methoxy-;2-Ethyl-4-amino-6-methoxy-s-triazine
• CAS NO: 701-78-0
• Molecular Formula: C₆H₁₀N₄O
• Molecular Weight: 154.17
• EINECS: 211-859-8
• Product Categories: API intermediates
• Mol File: 701-78-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 349.3°C at 760 mmHg
• Flash Point: 165°C
• Appearance: /
• Density: 1.202g/cm³
• Vapor Pressure: 4.76E-05mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: 2-AMINO-4-ETHYL-6-METHOXY-1,3,5-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-4-ETHYL-6-METHOXY-1,3,5-TRIAZINE(701-78-0)
• EPA Substance Registry System: 2-AMINO-4-ETHYL-6-METHOXY-1,3,5-TRIAZINE(701-78-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 701-78-0(Hazardous Substances Data)

Usage

General Description

2-Amino-4-ethyl-6-methoxy-1,3,5-triazine is a chemical compound with the molecular formula C6H10N4O. Also known as methyl ethyl benzoguanide or methoxy ethoxy ethyl guanide, this compound belongs to the class of organic compounds known as 1,3,5-triazines. It is a white, crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block for the synthesis of various compounds and is widely used in the chemical industry due to its versatile reactivity and potential applications. Additionally, it is known for its low volatility and non-corrosive nature, making it a valuable compound for many industrial processes.

InChI:InChI=1/C6H10N4O/c1-3-4-8-5(7)10-6(9-4)11-2/h3H2,1-2H3,(H2,7,8,9,10)

Relevant articles and documents

Process for the preparation of 2-amino-s-triazines

The present invention relates to a process for the preparation of 2-amino-s-triazines in three stages. In the first stage nitriles, alcohols and hydrogen chloride are reacted to form the corresponding imido-ester hydrochlorides. In the second stage, the imido-ester hydrochlorides are reacted with cyanamide in the aqueous phase to form the N-cyanimido-esters, which comprises carrying out the first stage in the presence of acetic acid esters and the second stage in an aqueous solution which has been brought to a pH value of 5-8 by addition of bases, and reacting the N-cyanimido-esters with O-alkylisourea, S-alkylisothiourea, guanidine or amidine salts in the presence of a base in the third stage. The 2-amino-s-triazines can be prepared in a high purity and with good yields in this manner.