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CAS

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40492-24-8

5-Pyrimidinamine, N-methyl(9CI), also known as N-methylpyrimidin-5-amine, is a chemical compound belonging to the family of pyrimidines and piperedinediones. It is an organic compound composed of carbon, hydrogen, and nitrogen, featuring a pyrimidinamine structure and a methyl group. 5-Pyrimidinamine, N-methyl(9CI) is frequently utilized as a building block or intermediate in the synthesis of more complex compounds, particularly in the pharmaceutical and medical industry. Due to the limited information on its toxicity and health effects, it is advised to handle 5-Pyrimidinamine, N-methyl- (9CI) with caution.

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  • 40492-24-8 Structure

  • Basic information

    1. Product Name: 5-Pyrimidinamine, N-methyl- (9CI)
    2. Synonyms: 5-Pyrimidinamine, N-methyl- (9CI);5-PyriMidinaMine, N-Methyl-;N-Methylpyrimidin-5-amine;5-MethylaMinopyriMidine;N-methyl-N-(5-pyrimidinyl)amine
    3. CAS NO:40492-24-8
    4. Molecular Formula: C5H7N3
    5. Molecular Weight: 109.12918
    6. EINECS: N/A
    7. Product Categories: PYRIMIDINE
    8. Mol File: 40492-24-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 229.986 °C at 760 mmHg
    3. Flash Point: 92.892 °C
    4. Appearance: /
    5. Density: 1.145 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-Pyrimidinamine, N-methyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Pyrimidinamine, N-methyl- (9CI)(40492-24-8)
    11. EPA Substance Registry System: 5-Pyrimidinamine, N-methyl- (9CI)(40492-24-8)

  • 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: 40492-24-8(Hazardous Substances Data)

40492-24-8 Usage

Uses

Used in Pharmaceutical Industry:
5-Pyrimidinamine, N-methyl(9CI) is used as a building block for the synthesis of more complex pharmaceutical compounds. Its chemical structure allows for the creation of various derivatives that can be employed in the development of new drugs and therapeutic agents.
Used in Medical Research:
5-Pyrimidinamine, N-methyl(9CI) is used as an intermediate in the synthesis of compounds for medical research. Its versatile structure enables the exploration of potential applications in the treatment of various diseases and conditions, contributing to the advancement of medical science.
Used in Drug Development:
5-Pyrimidinamine, N-methyl(9CI) is used as a key component in the development of new drugs. Its presence in the molecular structure of these compounds can influence their pharmacological properties, such as potency, selectivity, and bioavailability, making it a valuable asset in the drug discovery process.
Used in Chemical Synthesis:
5-Pyrimidinamine, N-methyl(9CI) is used as a reagent in various chemical synthesis processes. Its ability to form different types of chemical bonds with other molecules makes it a useful tool in the preparation of a wide range of chemical products, including those used in the pharmaceutical and medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 40492-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,9 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40492-24:
(7*4)+(6*0)+(5*4)+(4*9)+(3*2)+(2*2)+(1*4)=98
98 % 10 = 8
So 40492-24-8 is a valid CAS Registry Number.

40492-24-8SDS

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 N-methylpyrimidin-5-amine

1.2 Other means of identification

Product number -
Other names 5-Pyrimidinamine,N-methyl

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:40492-24-8 SDS

40492-24-8Upstream product

40492-24-8Downstream Products

40492-24-8Relevant articles and documents

P(III)/P(V)-Catalyzed Methylamination of Arylboronic Acids and Esters: Reductive C-N Coupling with Nitromethane as a Methylamine Surrogate

Li, Gen,Qin, Ziyang,Radosevich, Alexander T.

supporting information, p. 16205 - 16210 (2020/10/26)

The direct reductive N-arylation of nitromethane by organophosphorus-catalyzed reductive C-N coupling with arylboronic acid derivatives is reported. This method operates by the action of a small ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane P-oxide) together with a mild terminal reductant hydrosilane to drive the selective installation of the methylamino group to (hetero)aromatic boronic acids and esters. This method also provides for a unified synthetic approach to isotopically labeled N-methylanilines from various stable isotopologues of nitromethane (i.e., CD3NO2, CH315NO2, and 13CH3NO2), revealing this easy-to-handle compound as a versatile precursor for the direct installation of the methylamino group.

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