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2-Ethylamino-6-methyl-4-pyrimidinol is an organic compound with the molecular formula C6H10N4O. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring containing four carbon atoms and two nitrogen atoms. The compound features an ethylamine group (-NHCH2CH3) at the 2-position and a methyl group (-CH3) at the 6-position, with a hydroxyl group (-OH) attached to the 4-position. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antiviral and anticancer drugs. Its unique structure and properties make it a valuable building block in the development of new therapeutic agents.

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  • 5734-69-0 Structure
  • Basic information

    1. Product Name: 2-Ethylamino-6-methyl-4-pyrimidinol
    2. Synonyms: 2-Ethylamino-6-methyl-4-pyrimidinol;(2Z)-2-cyano-3-[4-(diMethylaMino)phenyl]-N-(4-hydroxyphenyl)prop-2-enaMide
    3. CAS NO:5734-69-0
    4. Molecular Formula: C7H11N3O
    5. Molecular Weight: 307.3465
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5734-69-0.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: 170-174 °C
    2. Boiling Point: 593°Cat760mmHg
    3. Flash Point: 312.4°C
    4. Appearance: /
    5. Density: 1.294g/cm3
    6. Vapor Pressure: 1.18E-14mmHg at 25°C
    7. Refractive Index: 1.701
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.92±0.50(Predicted)
    11. CAS DataBase Reference: 2-Ethylamino-6-methyl-4-pyrimidinol(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-Ethylamino-6-methyl-4-pyrimidinol(5734-69-0)
    13. EPA Substance Registry System: 2-Ethylamino-6-methyl-4-pyrimidinol(5734-69-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5734-69-0(Hazardous Substances Data)

5734-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5734-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5734-69:
(6*5)+(5*7)+(4*3)+(3*4)+(2*6)+(1*9)=110
110 % 10 = 0
So 5734-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H17N3O2/c1-21(2)16-7-3-13(4-8-16)11-14(12-19)18(23)20-15-5-9-17(22)10-6-15/h3-11,22H,1-2H3,(H,20,23)/b14-11-

5734-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylamino-4-hydroxy-6-methylpyrimidine

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2-ethylamino-6-methylpyrimidine

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:5734-69-0 SDS

5734-69-0Downstream Products

5734-69-0Relevant articles and documents

Continuous synthesis method of hydroxypyrimidine compound

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Paragraph 0012; 0030-0031, (2020/07/28)

The invention discloses a continuous synthesis method of a hydroxypyrimidine compound. The method comprises the steps: carrying out continuous reaction on organic amine and a 50% cyanamide aqueous solution in a micro-reactor, introducing the reaction solution into a liquid separator for continuous phase splitting, carrying out continuous ring closing on a guanidine solution and alpha-alkyl acetoacetate in a second micro-reactor, washing the reaction solution with water, and desolventizing to obtain a target product. The method is based on the concept of green chemistry, the comprehensive costof raw materials is far lower than that of traditional methods, no salt-containing wastewater is generated, and treatment is easy; traditional solid-liquid separation is avoided, automatic productionis facilitated, and the safety and environmental protection level of the device is improved; continuous synthesis is adopted, decomposition of an intermediate is avoided, the total yield is larger than 82%, and the product content reaches 98%.

Acetic acid derivatives and processes for their production

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, (2008/06/13)

A process for the preparation of a compound of formula: STR1 wherein R is an amino, hydrocarbylamino or dihydrocarbylamino radical, the hydrocarbylamino and dihydrocarbylamino radicals being unsubstituted, or substituted in the hydrocarbyl moiety with atoms or radicals which do not interfere with the process and Z is an acyl radical which comprises the steps of: (a) decarboxylating a compound of formula: STR2 to produce the corresponding 4-hydroxy-6-methyl-pyrimidine; and (B) TREATING THE CORRESPONDING 4-HYDROXY-6-METHYL PYRIMIDINE THUS PRODUCED WITH AN ACYLATING AGENT CAPABLE OF PROVIDING THE ACYL RADICAL Z; where both steps (a) and (b) are carried out in the same solvent or diluent.

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