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4-(ChloroMethyl)-2-(Methylthio)pyriMidine is a pyrimidine derivative with the molecular formula C7H9ClN2S. It features a chloromethyl group and a methylthio group attached to the pyrimidine ring, contributing to its reactivity and potential biological activities. This organic compound serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, making it a valuable building block for creating complex organic compounds.

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  • 944902-34-5 Structure
  • Basic information

    1. Product Name: 4-(ChloroMethyl)-2-(Methylthio)pyriMidine
    2. Synonyms: 4-(ChloroMethyl)-2-(Methylthio)pyriMidine
    3. CAS NO:944902-34-5
    4. Molecular Formula:
    5. Molecular Weight: 174.654
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 944902-34-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(ChloroMethyl)-2-(Methylthio)pyriMidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(ChloroMethyl)-2-(Methylthio)pyriMidine(944902-34-5)
    11. EPA Substance Registry System: 4-(ChloroMethyl)-2-(Methylthio)pyriMidine(944902-34-5)
  • 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: 944902-34-5(Hazardous Substances Data)

944902-34-5 Usage

Uses

Used in Pharmaceutical Industry:
4-(ChloroMethyl)-2-(Methylthio)pyriMidine is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its reactivity, due to the presence of the chloromethyl group, allows it to undergo multiple chemical reactions, facilitating the development of diverse drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(ChloroMethyl)-2-(Methylthio)pyriMidine serves as a key intermediate in the production of agrochemicals. Its ability to participate in various chemical reactions aids in the creation of effective compounds for agricultural applications.
Used in Organic Synthesis:
4-(ChloroMethyl)-2-(Methylthio)pyriMidine is utilized as a building block in organic synthesis. Its unique structure and reactivity make it suitable for the formation of a wide range of complex organic compounds, contributing to advancements in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 944902-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,9,0 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 944902-34:
(8*9)+(7*4)+(6*4)+(5*9)+(4*0)+(3*2)+(2*3)+(1*4)=185
185 % 10 = 5
So 944902-34-5 is a valid CAS Registry Number.

944902-34-5SDS

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 4-(chloromethyl)-2-methylsulfanylpyrimidine

1.2 Other means of identification

Product number -
Other names 2-METHYLSULFANYL-4-CHLOROMETHYLPYRIMIDINE

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:944902-34-5 SDS

944902-34-5Downstream Products

944902-34-5Relevant articles and documents

Novel Cyclic Urea Derivatives, Preparation Thereof and Pharmaceutical Use Thereof as Kinase Inhibitors

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Page/Page column 19, (2009/04/24)

Compounds of formula (I): wherein Ra, Rb, R, X1 and X2 are as defined in the disclosure, pharmaceutical compositions comprising said compounds, processes for making and methods of using the same are provided.

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