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2,3-Diiodo-pyridine, with the molecular formula C5H3I2N, is a pyridine derivative featuring two iodine atoms attached to the 2 and 3 positions on the pyridine ring. This chemical compound is recognized for its versatility in organic synthesis and as a reagent in a variety of chemical reactions, particularly due to its capacity to participate in halogenation reactions and serve as a source of iodine in organic transformations. Additionally, 2,3-diiodo-pyridine has garnered interest in the fields of medicinal chemistry, where it is considered a potential building block for the synthesis of pharmaceutical compounds.

83674-70-8

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83674-70-8 Usage

Uses

Used in Organic Synthesis:
2,3-Diiodo-pyridine is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for a range of chemical reactions, making it a valuable component in the synthesis of specialty chemicals and pharmaceuticals.
Used in Chemical Reactions as a Reagent:
In the realm of chemical reactions, 2,3-diiodo-pyridine serves as a reagent, particularly in processes that require halogenation. Its ability to participate in such reactions is instrumental in the formation of new chemical entities with potential applications in various industries.
Used in Medicinal Chemistry:
2,3-Diiodo-pyridine is explored in medicinal chemistry as a potential building block for the development of pharmaceutical compounds. Its structural features and reactivity make it a candidate for the creation of new drugs with specific therapeutic properties.
Used in Pharmaceutical Compounds Synthesis:
As a component in the synthesis of pharmaceutical compounds, 2,3-diiodo-pyridine contributes to the development of novel medications. Its presence in these compounds can influence their pharmacological activity, potentially leading to advancements in treatment options for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 83674-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,7 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83674-70:
(7*8)+(6*3)+(5*6)+(4*7)+(3*4)+(2*7)+(1*0)=158
158 % 10 = 8
So 83674-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H3I2N/c6-4-2-1-3-8-5(4)7/h1-3H

83674-70-8 Well-known Company Product Price

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  • Aldrich

  • (ADE000256)  2,3-Diiodo-pyridine  AldrichCPR

  • 83674-70-8

  • ADE000256-1G

  • 1,930.50CNY

  • Detail

83674-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diiodopyridine

1.2 Other means of identification

Product number -
Other names 2,3-Diiodo-pyridine

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:83674-70-8 SDS

83674-70-8Upstream product

83674-70-8Relevant academic research and scientific papers

Studies on Organometallic Compounds. II. Facile and Convenient Method for the Synthesis of Idoazines through Iododestannation of Trimethylstannylazines

Yamamoto, Yukata,Yanagi, Akihiko

, p. 1731 - 1737 (2007/10/02)

Trimethylsatannyl and bis(trimethylstannyl) derivatives of pyridine, quinoline, and isoquinoline were prepared from the corresponding halo and dihalo (chloro or bromo) derivatives and trimethylstannyl sodium, which was generated in situ from chlorotrimethylsatannane and sodium.These stannyl derivatives readily underwent iododestannation on treatment with iodine to produce the corresponding iodo and diiodo derivatives of pyridine, quinoline, and isoquinoline, respectively, in good yields.Keywords -trimethylsannylazine; bis(trimethylstannyl)azine; iodoazine; diiodoazine; iododestannation; trimethylstannyl sodium; chlorotrimethylstannane

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