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2,4-dichloro-6-(diazomethyl)-1,3,5-triazine is a synthetic compound characterized by its white to beige crystalline solid form. It is stable under normal conditions but can decompose explosively when subjected to heat or shock. 2,4-dichloro-6-(diazomethyl)-1,3,5-triazine's high reactivity is attributed to the presence of the diazomethyl group, which is instrumental in the formation of carbon-carbon bonds in organic synthesis. Due to its explosive nature and potential health hazards, it is crucial to handle and store 2,4-dichloro-6-(diazomethyl)-1,3,5-triazine with extreme caution and adherence to proper safety protocols.

4803-05-8

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4803-05-8 Usage

Uses

Used in Organic Synthesis:
2,4-dichloro-6-(diazomethyl)-1,3,5-triazine is used as a reagent for the introduction of the diazomethyl group into various molecules. Its reactivity is highly valued in the formation of carbon-carbon bonds, which is a critical step in the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4-dichloro-6-(diazomethyl)-1,3,5-triazine is used as a key intermediate in the synthesis of certain pharmaceuticals. Its ability to form carbon-carbon bonds makes it a valuable component in the development of new drugs and medicinal compounds.
Used in Chemical Research:
2,4-dichloro-6-(diazomethyl)-1,3,5-triazine is utilized in chemical research as a model compound to study the properties and reactions of diazomethyl groups. This helps in understanding the underlying mechanisms of various organic reactions and contributes to the advancement of synthetic chemistry.
Used in Material Science:
In material science, 2,4-dichloro-6-(diazomethyl)-1,3,5-triazine is employed in the development of novel materials with specific properties. Its reactivity allows for the creation of new polymers and composites with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4803-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4803-05:
(6*4)+(5*8)+(4*0)+(3*3)+(2*0)+(1*5)=78
78 % 10 = 8
So 4803-05-8 is a valid CAS Registry Number.

4803-05-8SDS

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 2,4-dichloro-6-diazomethyl-[1,3,5]triazine

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-6-diazomethyl-1,3,5-triazine

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:4803-05-8 SDS

4803-05-8Relevant academic research and scientific papers

REACTIVITY-IMPARTING COMPOUND, MANUFACTURING METHOD THEREOF, SURFACE REACTIVE SOLID USING REACTIVITY-IMPARTING COMPOUND, AND METHOD FOR MANUFACTURING SURFACE REACTIVE SOLID

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Paragraph 0044-0045; 0066, (2020/10/16)

PROBLEM TO BE SOLVED: To provide a reactivity-imparting compound that imparts reactivity enabling bonding between a solid and another material, wherein the reactivity-imparting compound can impart reactivity to the solid with high efficiency and wherein the bonding adhesion between the solid and another material is high, and to provide a method for manufacturing the same, a surface reactive solid using the same, and a method for manufacturing surface reactive solid. SOLUTION: There is provided a reactivity-imparting compound provided on a surface of a solid in order to bond between the solid and another material, wherein the reactivity-imparting compound is a compound having a triazine ring, an alkoxysilyl group (also including a case where an alkoxy group in the alkoxysilyl group is OH) and a diazomethyl group in one molecule. There are also provided a method for manufacturing the reactivity-imparting compound, a surface reactive solid using the same, and a method for manufacturing the surface reactive solid. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2020,JPOandINPIT

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