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6504-13-8

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6504-13-8 Usage

Description

4-(1H-BENZOIMIDAZOL-2-YL)-PHENOL, also known as HBBIP, is a phenolic compound with the molecular formula C13H10N2O. It features a benzimidazole ring, making it a significant building block for the synthesis of various drugs and bioactive molecules. HBBIP has demonstrated potential anti-inflammatory and antioxidant properties, as well as the ability to inhibit certain enzymes related to inflammation and oxidative stress. Its potential use in treating neurodegenerative diseases and cancer has also been explored, highlighting its diverse pharmacological activities and potential applications in drug development.

Uses

Used in Pharmaceutical Industry:
4-(1H-BENZOIMIDAZOL-2-YL)-PHENOL is used as a building block for the synthesis of various drugs and bioactive molecules due to its unique chemical structure and potential pharmacological properties.
Used in Anti-inflammatory Applications:
HBBIP is used as an anti-inflammatory agent for its potential to inhibit enzymes involved in inflammation, providing a basis for the development of treatments targeting inflammatory conditions.
Used in Antioxidant Applications:
4-(1H-BENZOIMIDAZOL-2-YL)-PHENOL is used as an antioxidant agent for its potential to combat oxidative stress, which can contribute to the development of various diseases and conditions.
Used in Neurodegenerative Disease Treatment:
HBBIP is used in research for the treatment of neurodegenerative diseases, given its potential to target mechanisms involved in these conditions, offering a new avenue for therapeutic intervention.
Used in Cancer Treatment:
4-(1H-BENZOIMIDAZOL-2-YL)-PHENOL is used in cancer research for its potential role in inhibiting cancer-related processes, making it a candidate for the development of novel cancer therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 6504-13-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,0 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6504-13:
(6*6)+(5*5)+(4*0)+(3*4)+(2*1)+(1*3)=78
78 % 10 = 8
So 6504-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O/c16-10-7-5-9(6-8-10)13-14-11-3-1-2-4-12(11)15-13/h1-8,16H,(H,14,15)

6504-13-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,3-dihydrobenzimidazol-2-ylidene)cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-benzimidazol-2-ylphenol

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:6504-13-8 SDS

6504-13-8Relevant articles and documents

Systemic study on fluorescent switching systems composed of naphthopyran and benzimidazole in solution and film forms

He, Yi,Wang, Guang,Wang, Mingxin

, p. 19 - 28 (2016)

The fluorescent photo-switching systems were prepared based on fluorescent benzimidazole and photochromic naphthopyran. Naphthopyran in this systems displayed excellent photochromic performance in tetrahydrofuran solutions and in PMMA films. The fluoresce

Stability constants of Ni(II)- and Cu(II)-N-heterocycle complexes according to spectrophotometric data

Badhe, Samata,Tekade, Pradip,Bajaj, Sonal,Thakare, Shrikant

, p. 2254 - 2258 (2015)

The interaction of Ni(II) and Cu(II) with ethyl 4-(4-hydroxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine- 5-carboxylate [Ligand 1], 4-(1H-benzimidazol-2-yl)phenol [Ligand 2], and 2-(3-phenylamino- 4,5-dihydro-1,2-oxazol-5-yl)phenol [Ligand 3] have been studied by spectrophotometric technique at 0.01 M ionic strength and 28°C in 70% dioxane - water mixture. The data obtained were used to estimate the stability constant of these ligands. Spectrophotometric investigation of Ni(II) and Cu(II) complexes with these ligands shows 1: 1 complex formation. The formation of complexes has been studied by Job's variation method. The values of conditional stability constants of Cu(II) complexes are greater than the corresponding Ni(II) complexes. The greater value of stability constant of Cu(II) complexes may be due to the fact of more stable nature of Cu(II). The value of stability constant of Cu(II) - Ligand 2 complex is greater than that of Cu(II)-Ligand 1 and Cu(II)-Ligand 3. The same of Ni(II)-Ligand 3 complex is greater than that of Ni(II)-Ligand 1 and Ni(II)-Ligand 2.

[Diaquo{bis(p-hydroxybenzoato-κ1O1)}(1-methylimidazole- κ1N1)}copper(II)]: Synthesis, crystal structure, catalytic activity and DFT study

Brahman, Dhiraj,Chhetri, Sailesh,Kamath, Amarjit,McArdle, Patrick,Sinha, Biswajit

, (2021/09/04)

Metal-organic hybrid complexes often exhibit large surface area, pore volume, fascinating structures and potential applications including catalytic applications. Hence a new metal-organic hybrid complex [Diaquo{bis(p-hydroxybenzoato-κ1O1)}(1-methylimidazole- κ1N1)}copper(II)] was synthesized using conventional method. Physico-chemical characterization of the complex was performed with FTIR spectroscopy, single crystal X-ray diffraction, TGA, EPR and FESEM. Single crystal X-ray diffraction study suggests it to be three dimensional with space group P212121 (orthorhombic). The crystal achieves its three-dimensional structure and stability through extensive intermolecular hydrogen bonding. Hirshfeld surface analysis, catalytic activity and DFT study of the complex was also performed. The synthesized complex acts as good catalyst in benzimidazole synthesis with good recyclability as catalyst up to 5th run.

Solvent-dependent metal-free chemoselective synthesis of benzimidazoles and 1,3,5-triarylbenzenes from 2-amino anilines and aryl alkyl ketones catalyzed by I2

Ding, Yuxin,Ma, Renchao,Ma, Yongmin

supporting information, (2021/04/09)

A solvent-dependent I2-catalyzed chemoselective reaction was developed for the synthesis of benzimidazoles and 1,3,5-triarylbenzenes via the annulation of 2-amino anilines and aryl alkyl ketones or the cyclization of aryl alkyl ketones, respectively. With 1,4-dioxane as the solvent, sequential C[sbnd]N bond formation followed by C(CO)-C(CH3) bond cleavage leads to the formation of benzimidazoles in a highly selective manner while aldol-type self-condensation of aryl alkyl ketones predominates using PhNO2 or PhCl as the solvent to afford 1,3,5-triarylbenzenes.

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