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2-IODO-1H-BENZOIMIDAZOLE, with the molecular formula C7H5IN2, is a derivative of benzimidazole that incorporates an iodine atom. This chemical compound has garnered attention for its potential applications in pharmaceutical and agricultural sectors due to its notable biological and therapeutic properties.

27692-04-2

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27692-04-2 Usage

Uses

Used in Pharmaceutical Applications:
2-IODO-1H-BENZOIMIDAZOLE is used as an antimicrobial and antifungal agent for its effectiveness against a range of microorganisms. Its unique structure and properties make it a promising candidate for the development of new therapeutic agents.
Used in Agricultural Applications:
In the agricultural industry, 2-IODO-1H-BENZOIMIDAZOLE is used as a bioactive compound for its potential to combat various plant pathogens, thereby enhancing crop protection and yield.
Used in Organic Synthesis:
2-IODO-1H-BENZOIMIDAZOLE is utilized as a building block in the synthesis of other organic compounds, contributing to the creation of novel chemical entities with potential applications in various fields.
2-IODO-1H-BENZOIMIDAZOLE's versatility and the ongoing research into its properties suggest that 2-IODO-1H-BENZOIMIDAZOLE could play a significant role in future advancements in medicine and agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 27692-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,9 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27692-04:
(7*2)+(6*7)+(5*6)+(4*9)+(3*2)+(2*0)+(1*4)=132
132 % 10 = 2
So 27692-04-2 is a valid CAS Registry Number.

27692-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazole,2-iodo

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:27692-04-2 SDS

27692-04-2Relevant academic research and scientific papers

Access to aromatic ring-fused benzimidazoles using photochemical substitutions of the benzimidazol-2-yl radical

Oconnell, Joanne M.,Moriarty, Eoin,Aldabbagh, Fawaz

, p. 3371 - 3377,7 (2012/12/12)

Photochemical five-, six-, and seven-membered cyclizations from 2-iodo-1-(ω-arylalkyl)-1H-benzimidazoles are described. This method of producing aromatic ring-fused benzimidazoles is significantly more efficient than literature radical protocols using chemical initiators, although 2-iodo-1-(ω-pyridin-2-ylalkyl)-1H-benzimidazoles preferentially undergo a nucleophilic ipso-substitution onto the benzimidazole-2-position.

Access to aromatic ring-fused benzimidazoles using photochemical substitutions of the benzimidazol-2-yl radical

Oconnell, Joanne M.,Moriarty, Eoin,Aldabbagh, Fawaz

, p. 3371 - 3377 (2013/01/15)

Photochemical five-, six-, and seven-membered cyclizations from 2-iodo-1-(ω-arylalkyl)-1H-benzimidazoles are described. This method of producing aromatic ring-fused benzimidazoles is significantly more efficient than literature radical protocols using chemical initiators, although 2-iodo-1-(ω-pyridin-2-ylalkyl)-1H-benzimidazoles preferentially undergo a nucleophilic ipso-substitution onto the benzimidazole-2-position. Georg Thieme Verlag Stuttgart - New York.

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