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40951-05-1

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40951-05-1 Usage

Description

(2E)-3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide is a chemical compound with the molecular formula C17H21NO3. It is an amide that features a benzodioxole ring and a diethylpropenyl group. (2E)-3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide is primarily utilized in research and pharmaceutical applications, particularly for the development of drugs targeting the central nervous system. Its unique structure and potential biological activities contribute to its value in understanding and treating various neurological conditions. Due to its complex nature and possible biological effects, it is essential to handle and use this chemical with care, adhering to proper safety measures and guidelines.

Uses

Used in Pharmaceutical Research and Development:
(2E)-3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide is used as a research compound for the development of drugs targeting the central nervous system. Its specific properties and potential biological activities make it a valuable tool in understanding and treating various neurological conditions.
Used in Drug Discovery:
In the pharmaceutical industry, (2E)-3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide is used as a lead compound in drug discovery. Its unique structure and potential interactions with biological targets make it a promising candidate for the development of new therapeutic agents.
Used in Neurological Research:
(2E)-3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide is used as a research tool in the study of neurological conditions. Its potential biological activities and interactions with the central nervous system contribute to a better understanding of these conditions and the development of effective treatments.
Used in Safety and Toxicology Studies:
Due to its complex structure and potential for biological activity, (2E)-3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide is also used in safety and toxicology studies. These studies are crucial for evaluating the safety and potential side effects of this compound before it can be used in clinical applications or as a component of pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 40951-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40951-05:
(7*4)+(6*0)+(5*9)+(4*5)+(3*1)+(2*0)+(1*5)=101
101 % 10 = 1
So 40951-05-1 is a valid CAS Registry Number.

40951-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,3-benzodioxol-5-yl)-N,N-diethylprop-2-enamide

1.2 Other means of identification

Product number -
Other names 3,4-Methylendioxy-zimtsaeure-N,N-diaethylamid

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:40951-05-1 SDS

40951-05-1Downstream Products

40951-05-1Relevant articles and documents

Piperine derivative as well as preparation method and application thereof

-

Paragraph 0142; 0263-0265, (2020/05/08)

The invention provides a piperine derivative as well as a preparation method and an application thereof. The piperine derivative is a compound shown as a formula (I), or a salt thereof, or a stereoisomer thereof, or a hydrate thereof. The compound provided by the invention can effectively protect nerve cells and improve the survival rate of the nerve cells, so that the compound provided by the invention can effectively treat neurodegenerative diseases and can be used for preparing medicines for treating the neurodegenerative diseases.

Indium-mediated microwave-assisted one-pot synthesis of α,β-unsaturated amides

Feng, Sunlin,Jiang, Shilei,Zhang, Zhiying,Yu, Xiaochun

experimental part, p. 392 - 394 (2010/11/18)

A stereoselective synthesis of α,β-unsaturated-N,N-diethyl amides was achieved by a one-pot reaction of triphenylphosphine, an aromatic aldehyde, and N,N-diethyl chloroacetamide in the presence of indium under microwave-assisted and solvent-free condition.

Synthesis of α β,-unsaturated amide via phosphonium ylide

Jiang, Shilei,Yang, Kefeng,Yu, Xiaochun

supporting information; experimental part, p. 1759 - 1767 (2009/11/30)

A series of ,-unsaturated amides were prepared by the Wittig reaction of N,N-diethylamidemethylenetriphenylphosphorane ylide with aldehydes with moderate to good yields. Copyright Taylor & Francis Group, LLC.

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