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3034-62-6

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3034-62-6 Usage

Description

2-Iodoimidazole is an organic compound with the molecular formula C3H3IN2, featuring an imidazole ring with an iodine atom at the 2nd position. It is a versatile chemical intermediate and reagent in various chemical reactions and synthesis processes.

Uses

Used in Pharmaceutical Industry:
2-Iodoimidazole is used as a reactant for the alkylation process, leading to the formation of alkyl derivatives with antibacterial activity. These derivatives can be further utilized in the development of new antibiotics and antimicrobial agents.
Used in Chemical Synthesis:
2-Iodoimidazole is used as a reactant in the iodination of N-tritylimidazole, which is an essential step in the synthesis of various organic compounds and pharmaceuticals.
Used in Photochemistry:
In the field of photochemistry, 2-Iodoimidazole is employed as a reactant in photochemical intramolecular aromatic substitutions. This process allows for the formation of novel aromatic compounds with unique properties and potential applications.
Used in Organic Synthesis:
2-Iodoimidazole is used as a reactant in the synthesis of cyclopentapyrazines through a thermolysis process. These cyclopentapyrazine compounds have potential applications in various fields, including pharmaceuticals, materials science, and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 3034-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3034-62:
(6*3)+(5*0)+(4*3)+(3*4)+(2*6)+(1*2)=56
56 % 10 = 6
So 3034-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H3IN2/c4-3-5-1-2-6-3/h1-2H,(H,5,6)

3034-62-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (H51868)  2-Iodoimidazole, 96%   

  • 3034-62-6

  • 250mg

  • 1058.0CNY

  • Detail
  • Alfa Aesar

  • (H51868)  2-Iodoimidazole, 96%   

  • 3034-62-6

  • 1g

  • 2700.0CNY

  • Detail
  • Aldrich

  • (641081)  2-Iodoimidazole  97%

  • 3034-62-6

  • 641081-1G

  • 1,832.22CNY

  • Detail
  • Aldrich

  • (641081)  2-Iodoimidazole  97%

  • 3034-62-6

  • 641081-5G

  • 7,014.15CNY

  • Detail

3034-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodoimidazole

1.2 Other means of identification

Product number -
Other names 2-Iodo-1H-imidazole

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:3034-62-6 SDS

3034-62-6Relevant articles and documents

FRICTIONLESS MOLECULAR ROTARY MOTORS

-

Page/Page column 29, (2010/02/17)

A rotaxane consisting of a cucurbituril and an uncharged guest molecule, having low or null affinity therebetween is provided as well as processes for providing the same. Various uses as energy converters (“frictionless” molecular motors), biochips and biosensors using the same are also provided.

A comparison of microwave-accelerated and conventionally heated iodination reactions of some arenes and heteroarenes, using ortho-periodic acid as the oxidant

Sosnowski, Maciej,Skulski, Lech

, p. 401 - 406 (2007/10/03)

A fast and simple method for the oxidative iodination of some activated arenes and heteroarenes, either under microwave irradiation or by conventional heating, is reported, using diiodine and ortho-periodic acid as the oxidant. The reactions were carried out in hot 95% ethanol under a reflux condenser. For the microwave assisted reactions, the reaction times were always notably shortened, but the yields were nearly the same as those afforded by the conventional method.

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