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[3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL is a complex organic compound characterized by the presence of an imidazole ring, which is a heterocyclic aromatic organic compound. This ring is fused with a methanol group, and the molecule is further modified by the attachment of an ethoxy-propyl group. The combination of these functional groups suggests that [3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL may exhibit a range of biological activities and could be utilized in various applications, particularly in the fields of pharmaceuticals and organic synthesis.

226931-06-2

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226931-06-2 Usage

Uses

Used in Pharmaceutical Industry:
[3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL is used as a potential active pharmaceutical ingredient for its possible antifungal and antibacterial properties. The imidazole ring is known for its biological activity, and the additional ethoxy-propyl and methanol groups may enhance these properties, making it a candidate for the development of new antimicrobial agents.
Used in Organic Synthesis:
In the field of organic synthesis, [3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL can be used as a building block or intermediate in the synthesis of more complex organic compounds. Its unique structure, including the imidazole ring and the ethoxy-propyl chain, may allow for the creation of novel molecules with specific functions or properties.
Used in Research and Development:
[3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL is also used in research and development for further exploration of its potential applications. Given the compound's structure and the known properties of imidazoles, it may be of interest to scientists looking to understand its interactions with biological systems or to develop new methodologies for its synthesis and modification.
While the specific uses of [3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL are not exhaustively listed in the provided materials, the potential applications mentioned are based on the compound's structural features and the known properties of similar compounds. Further research would be necessary to validate these uses and to explore additional applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 226931-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,3 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 226931-06:
(8*2)+(7*2)+(6*6)+(5*9)+(4*3)+(3*1)+(2*0)+(1*6)=132
132 % 10 = 2
So 226931-06-2 is a valid CAS Registry Number.

226931-06-2SDS

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 [3-(3-ETHOXY-PROPYL)-3H-IMIDAZOL-4-YL]-METHANOL

1.2 Other means of identification

Product number -
Other names -

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:226931-06-2 SDS

226931-06-2Upstream product

226931-06-2Downstream Products

226931-06-2Relevant articles and documents

Efficient synthesis of 1-substituted-5-hydroxymethylimidazole derivatives: Clean oxidative cleavage of 2-mercapto group

Hyok Chang, Jay,Woong Lee, Kyu,Hyun Nam, Do,Sup Kim, Won,Shin, Hyunik

, p. 674 - 676 (2013/09/06)

1-Substituted-5-hydroxymethylimidazoles were prepared through green desulfurization of their 2-mercapto derivatives by the treatment of 30% hydrogen peroxide in the presence of a catalytic amount of transition metal catalysts.

Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof

-

, (2008/06/13)

The present invention relates to a novel imidazole derivative represented by formula (1) which shows an inhibitory activity against farnesyl transferase or pharmaceutically acceptable salts or isomers thereof, in which A, n1and Y are defined in the specification; to a process for preparation of the compound of formula (1); to intermediates which are used in the preparation of the compound of formula (1); and to a pharmaceutical composition comprising the compound of formula (1) as an active ingredient.

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