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3,4-Diiodopyrazole is a pyrazole derivative with the molecular formula C3H2I2N2, featuring two iodine atoms attached to the 3 and 4 positions of the pyrazole ring. This chemical compound is recognized for its unique structural properties and serves as a versatile synthetic intermediate in various fields, including organic synthesis, medicinal chemistry, pharmaceuticals, agrochemicals, and material science.

6645-70-1

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6645-70-1 Usage

Uses

Used in Organic Synthesis:
3,4-Diiodopyrazole is used as a building block in organic synthesis for the preparation of various biologically active molecules. Its unique structural properties make it a valuable component in the creation of new compounds with potential applications in various industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3,4-Diiodopyrazole is utilized as a key intermediate for the development of pharmaceuticals. Its presence in the molecular structure can contribute to the enhancement of biological activity and therapeutic effects of drug candidates.
Used in Pharmaceutical Industry:
3,4-Diiodopyrazole is used as a synthetic intermediate in the pharmaceutical industry for the preparation of drugs with potential therapeutic applications. Its unique structural features allow for the design and synthesis of novel drug molecules with improved efficacy and selectivity.
Used in Agrochemical Industry:
In agrochemicals, 3,4-Diiodopyrazole is employed as a building block for the synthesis of bioactive molecules with potential applications in pest control and crop protection. Its unique properties can contribute to the development of more effective and environmentally friendly agrochemical products.
Used in Material Science:
3,4-Diiodopyrazole is used in material science for the development of new materials with specific properties. Its unique structural features can be leveraged to create materials with improved performance in various applications, such as sensors, catalysts, or advanced materials for electronic devices.
Overall, 3,4-Diiodopyrazole's versatility and unique structural properties make it a valuable compound in multiple industries, driving research and development efforts to harness its potential in creating innovative products and solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 6645-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6645-70:
(6*6)+(5*6)+(4*4)+(3*5)+(2*7)+(1*0)=111
111 % 10 = 1
So 6645-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H2I2N2/c4-2-1-6-7-3(2)5/h1H,(H,6,7)

6645-70-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diiodo-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3,4-Diiod-pyrazol

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:6645-70-1 SDS

6645-70-1Upstream product

6645-70-1Downstream Products

6645-70-1Relevant academic research and scientific papers

Mild regioselective iodination of pyrazoles using n-butyltriphenylphosphonium peroxodisulfate

Gorjizadeh,Afshari,Naseh

, p. 1931 - 1934 (2016/10/04)

A practical, efficient and inexpensive method of synthesis of iodopyrazoles by the reaction of pyrazoles with iodine using n-butyltriphenylphosphonium peroxodisulfate as an oxidant at room temperature is reported. The use of n-butyltriphenylphosphonium peroxodisulfate is feasible due to its easy preparation and handling, high stability and activity.

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