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2,4-Dichlorobenzenediazonium tetrafluoroborate is a chemical compound with the formula C6H3Cl2BF4N2. As an organohalogen compound, it has two chlorine atoms substituted in the benzene ring. It is typically used in organic chemistry as a diazonium salt. Diazonium salts are generally useful in reactions that result in the substitution of new groups into molecules for the creation of a wide variety of complex organic compounds. Typically, 2,4-Dichlorobenzenediazonium tetrafluoroborate is stored under special conditions to prevent it from decomposing, since it can become unstable and potentially explode under certain conditions. As a result, it is handled with care to ensure safe usage.

21872-70-8

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21872-70-8 Usage

Uses

Used in Organic Chemistry:
2,4-Dichlorobenzenediazonium tetrafluoroborate is used as a diazonium salt for facilitating the substitution of new groups into molecules. This is particularly important in the synthesis of complex organic compounds, where the diazotization reaction allows for the introduction of various functional groups, enhancing the versatility of the final products.
Used in Research and Development:
In the field of research and development, 2,4-Dichlorobenzenediazonium tetrafluoroborate is used as a reagent in various chemical reactions. Its ability to participate in diazotization reactions makes it a valuable tool for exploring new chemical pathways and synthesizing novel compounds with potential applications in various industries, such as pharmaceuticals, materials science, and agrochemicals.
Used in Industrial Applications:
2,4-Dichlorobenzenediazonium tetrafluoroborate is used as a key intermediate in the production of certain industrial chemicals. Its role in diazotization reactions allows for the creation of new compounds that can be further processed or used as building blocks in the synthesis of more complex molecules, contributing to the development of new materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 21872-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,7 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21872-70:
(7*2)+(6*1)+(5*8)+(4*7)+(3*2)+(2*7)+(1*0)=108
108 % 10 = 8
So 21872-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl2N2.BF4/c7-4-1-2-6(10-9)5(8)3-4;2-1(3,4)5/h1-3H;/q+1;-1

21872-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dichlorobenzenediazonium,tetrafluoroborate

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-benzenediazonium,tetrafluoroborate

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:21872-70-8 SDS

21872-70-8Upstream product

21872-70-8Relevant academic research and scientific papers

Copper-mediated tandem ring-opening/cyclization reactions of cyclopropanols with aryldiazonium salts: Synthesis of: N -arylpyrazoles

Liu, Jidan,Xu, Erjie,Jiang, Jinyuan,Huang, Zeng,Zheng, Liyao,Liu, Zhao-Qing

supporting information, p. 2202 - 2205 (2020/02/26)

A general method for the synthesis of structurally diverse N-arylpyrazoles from readily available cyclopropanols and aryldiazonium salts is disclosed. The reaction was conducted at room temperature within minutes with a broad substrate scope and excellent regioselectivity.

NEW 1,2,4-TRIAZOLE-3-CARBOXAMIDE DERIVATIVES

-

Page/Page column 5; 12, (2010/10/20)

The invention relates to new 1,2,4-triazole-3-carboxamide derivatives, as well as to their use for the treatment of diseases in which cannabinoid receptors are involved.

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