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2-(1-METHYL-1H-IMIDAZOL-2-YL)-PHENOL is a chemical compound with the molecular formula C10H10N2O. It is a phenolic compound with an imidazole ring attached to the phenol group, which gives it unique properties and potential applications.
Used in Pharmaceutical Industry:
2-(1-METHYL-1H-IMIDAZOL-2-YL)-PHENOL is used as a pharmaceutical ingredient for its potential therapeutic effects.
Used in Antimicrobial Applications:
2-(1-METHYL-1H-IMIDAZOL-2-YL)-PHENOL is used as an antimicrobial agent for its ability to inhibit the growth of microorganisms.
Used in Antioxidant Applications:
2-(1-METHYL-1H-IMIDAZOL-2-YL)-PHENOL is used as an antioxidant for its potential to protect against oxidative stress and damage.
Used in Organic Synthesis:
2-(1-METHYL-1H-IMIDAZOL-2-YL)-PHENOL is used as a versatile chemical in the field of organic synthesis for its potential to be used in the creation of new compounds.
Used in Material Science:
2-(1-METHYL-1H-IMIDAZOL-2-YL)-PHENOL is used in material science for its potential applications in the development of new materials with unique properties.

52755-94-9

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52755-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52755-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,5 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52755-94:
(7*5)+(6*2)+(5*7)+(4*5)+(3*5)+(2*9)+(1*4)=139
139 % 10 = 9
So 52755-94-9 is a valid CAS Registry Number.

52755-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(3-methyl-1H-imidazol-2-ylidene)cyclohexa-2,4-dien-1-one

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:52755-94-9 SDS

52755-94-9Relevant academic research and scientific papers

FOUR-COORDINATE BORON COMPOUNDS

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Page/Page column 29, (2016/11/21)

A compound having a four-coordinate boron atom to which is connected a first C3-C25 substituent, a second C3-C25 substituent and a bridging substituent comprising from eight to forty non-hydrogen atoms and havin

Simple heteroatom engineering for tuning the triplet energy of organometallic host materials for red, green and blue phosphorescent organic light-emitting diodes

Oh, Chan Seok,Lee, Chil Won,Lee, Jun Yeob

supporting information, p. 3875 - 3877 (2013/07/19)

Triplet energy tuning from 2.48 eV to 2.94 eV by just a simple change of heteroatom in the ligand structure of Be complexes was studied using azole based triplet host materials. Three Be organometallic host materials with azole type ligands were synthesized and could be used as the host materials from red to deep blue phosphorescent organic light-emitting diodes. High quantum efficiency was obtained in red, green, blue and deep blue devices using the Be complexes. In particular, a high quantum efficiency of 26.1% was achieved in blue phosphorescent organic light-emitting diodes.

Intramolecular catalysis of phosphodiester hydrolysis by two imidazoles

Orth, Elisa S.,Brandao, Tiago A.S.,Souza, Bruno S.,Pliego, Josefredo R.,Vaz, Boniek G.,Eberlin, Marcos N.,Kirby, Anthony J.,Nome, Faruk

supporting information; scheme or table, p. 8513 - 8523 (2010/08/05)

Two imidazole groups act together to catalyze the hydrolysis of the phosphodiester bis(2-(1-methyl-1H-imidazolyl)phenyl) phosphate (BMIPP). A full investigation involving searching computational and electrospray ionization (ESI-MS-/MS) and ultra mass spec

Intramolecular acid-base catalysis of a phosphate diester: Modeling the ribonuclease mechanism

Orth, Elisa S.,Brandao, Tiago A. S.,Milagre, Humberto M. S.,Eberlin, Marcos N.,Nome, Faruk

, p. 2436 - 2437 (2008/09/17)

The hydrolysis of the phosphate diester bis(2-(1-methyl-1H-imidazolyl)phenyl) phosphate BMIPP was evaluated as an intramolecular model for the ribonuclease A mechanism. Kinetic and thermodynamic data, isotope effects and ESI-MS and ESI-MS/MS analysis supp

Nickel/zinc-mediated alkyl carbon-oxygen bond cleavage of alkyl aryl ethers

Maeyama, Katsuya,Kobayashi, Masato,Yonezawa, Noriyuki

, p. 869 - 875 (2007/10/03)

Alkyl carbon-oxygen bonds of alkyl aryl ethers bearing suitable coordination sites were efficiently cleaved by treatment with nickel(II) chloride and zinc in p-xylene under neutral conditions.

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