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96605-65-1

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96605-65-1 Usage

Description

(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide is a synthetic amide derivative with the molecular formula C17H22N2O2. It is a chemical compound known for its potential use as a fluorescent tracer in biological research applications. (E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide possesses certain biochemical and physiological properties that make it suitable for various medical and pharmaceutical applications, including drug development and disease research. Its unique structure allows it to be utilized as a reagent in chemical synthesis and as a probe for studying biological processes. Furthermore, it is considered a potential analytical standard and reference material for chromatography and spectrometry analysis.

Uses

Used in Biological Research:
(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide is used as a fluorescent tracer for visualizing and tracking specific biological processes and interactions within living organisms. Its fluorescent properties enable researchers to monitor cellular activities and study the behavior of biomolecules in real-time.
Used in Drug Development:
In the pharmaceutical industry, (E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide serves as a valuable compound in the development of new drugs. Its unique structure and properties can be exploited to design and synthesize novel therapeutic agents targeting various diseases.
Used in Disease Research:
(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide is also utilized in the study of various diseases, particularly those related to cellular and molecular mechanisms. It can help researchers understand the underlying causes of diseases and identify potential therapeutic targets.
Used as a Reagent in Chemical Synthesis:
(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide is employed as a reagent in chemical synthesis, where it can be used to produce a variety of other chemical compounds with different applications.
Used as a Probe for Studying Biological Processes:
As a probe, this compound can be used to investigate specific biological processes, such as enzyme activity, protein-protein interactions, and signal transduction pathways. This can provide valuable insights into the mechanisms of various biological phenomena.
Used as an Analytical Standard and Reference Material:
(E)-N-(3-(3-(Dimethylamino)acryloyl)phenyl)-N-methylacetamide is considered a potential analytical standard and reference material for chromatography and spectrometry analysis. Its use in these techniques can help ensure accurate and reliable results in various analytical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 96605-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,6,0 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96605-65:
(7*9)+(6*6)+(5*6)+(4*0)+(3*5)+(2*6)+(1*5)=161
161 % 10 = 1
So 96605-65-1 is a valid CAS Registry Number.

96605-65-1SDS

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 N-[3-[(E)-3-(dimethylamino)prop-2-enoyl]phenyl]-N-methylacetamide

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:96605-65-1 SDS

96605-65-1Relevant articles and documents

Polymorphs of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-α]-pyrimidin-7-yl}phenyl)acetamide and compositions and methods related thereto

-

, (2008/06/13)

Polymorphs of N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-α]-pyrimidin-7-yl}phenyl)acetamide (Compound 1), and use of the same as a sedative-hypnotic, anxiolytic, anticonvulsant, and skeletal muscle relaxant agent. Processes for making the same, as well as related compositions and methods are also disclosed, particularly with regard to treatment of insomnia. A polymorph Form I possessing exception physical and heat stability is provided. A polymorph Form II

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