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1-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1244949-16-3

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1244949-16-3 Usage

Molecular Weight

267.32 g/mol

Functional Groups

Ethanone (ketones)
Phenyl (aromatic ring)
Methoxy (ether)
Imidazol (heterocyclic)
Methyl (alkyl)

Structure

Central ethanone group
Attached phenyl ring
3-methoxy group on the phenyl ring
4-(4-methyl-1H-imidazol-1-yl) substituent on the phenyl ring

Potential Applications

Pharmaceutical industry
Drug development

Chemical Properties

Reactivity with various reagents
Valuable building block for complex organic molecules

Research Interest

Researchers and scientists in various fields
Study of structure and properties

Solubility

Soluble in organic solvents like ethanol, methanol, and acetone
Insoluble in water

Stability

Stable under normal conditions
May decompose under extreme temperatures or with strong acids/bases

Melting Point

Varies depending on the specific compound, but generally has a high melting point due to the presence of aromatic and heterocyclic groups

Boiling Point

Varies depending on the specific compound, but generally has a high boiling point due to the presence of aromatic and heterocyclic groups

Density

Typically less dense than water, but the exact value depends on the specific compound

Optical Properties

May exhibit UV-Vis absorption due to the presence of the phenyl and imidazol groups
May have potential for fluorescence or phosphorescence depending on the specific compound

Synthesis

Can be synthesized through various organic reactions, such as condensation, substitution, or addition reactions involving the appropriate precursors and reagents

Hazards

May be harmful if swallowed, inhaled, or absorbed through the skin
May cause irritation to the eyes, skin, or respiratory system
Proper handling and storage are necessary to minimize risks

Check Digit Verification of cas no

The CAS Registry Mumber 1244949-16-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,9,4 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1244949-16:
(9*1)+(8*2)+(7*4)+(6*4)+(5*9)+(4*4)+(3*9)+(2*1)+(1*6)=173
173 % 10 = 3
So 1244949-16-3 is a valid CAS Registry Number.

1244949-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]ethanone

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:1244949-16-3 SDS

1244949-16-3Relevant academic research and scientific papers

Design and synthesis of novel methoxypyridine-derived gamma-secretase modulators

Barnes, Keith D.,Buckle, Ronald N.,Chen, Xinchao,Herr, R. Jason,Johnson, Graham,Lin, Juinn H.,Mayhew, Nicholas J.,Mobley, William C.,Nguyen, Phuong,Paquette, William D.,Rynearson, Kevin D.,Sakwa, Samuel A.,Tanzi, Rudolph E.,Wagner, Steven L.,Yang, Jinhai

, (2020/09/22)

The evolution of gamma-secretase modulators (GSMs) through the introduction of novel heterocycles with the goal of aligning activity for reducing the levels of Aβ42 and properties consistent with a drug-like molecule are described. The insertion of a methoxypyridine motif within the tetracyclic scaffold provided compounds with improved activity for arresting Aβ42 production as well as improved properties, including solubility. In vivo pharmacokinetic analysis demonstrated that several compounds within the novel series were capable of crossing the BBB and accessing the therapeutic target. Treatment with methoxypyridine-derived compound 64 reduced Aβ42 levels in the plasma of J20 mice, in addition to reducing Aβ42 levels in the plasma and brain of Tg2576 mice.

COMPOUNDS AND USES THEREOF IN MODULATING LEVELS OF VARIOUS AMYLOID BETA PEPTIDE ALLOFORMS

-

, (2012/01/14)

The invention provides a novel compound having a structure corresponding to Formula (I): (A)-(B)-(C)-(D) or a pharmaceutically acceptable salt or prodrug thereof and methods for using them.

Pyridazine-derived γ-secretase modulators

Wan, Zehong,Hall, Adrian,Jin, Yun,Xiang, Jia-Ning,Yang, Eric,Eatherton, Andrew,Smith, Beverley,Yang, Guang,Yu, Haihua,Wang, Ju,Ye, Liang,Lau, Lit-Fui,Yang, Ting,Mitchell, William,Cai, Wei,Zhang, Xiaomin,Sang, Yingxia,Wang, Yonghui,Tong, Zhaolong,Cheng, Ziqiang,Hussain, Ishrut,Elliott, John D.,Matsuoka, Yasuji

scheme or table, p. 4016 - 4019 (2011/08/06)

SAR of a novel series of pyridazine-derived γ-secretase modulators is described. Compound 25 was found to be a potent modulator in vitro, which on further profiling, was found to decrease Aβ42 and Aβ40, and maintain the levels of total Aβ. Furthermore, 25

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