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(2E)-N-prop-2-en-1-ylbut-2-enamide, also known as N-allyl-2-butene-1-amide, is a chemical compound with the molecular formula C8H15NO. It is classified as an alkene amide and is known for its reactivity as a Michael acceptor, making it an important building block in the synthesis of various organic compounds.

69833-27-8

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69833-27-8 Usage

Uses

Used in Organic Synthesis:
(2E)-N-prop-2-en-1-ylbut-2-enamide is used as a building block for the synthesis of various organic compounds due to its reactivity as a Michael acceptor.
Used in Pharmaceutical Research and Development:
(2E)-N-prop-2-en-1-ylbut-2-enamide is used as a starting material in the synthesis of potential drug candidates, contributing to the development of new medications.
Used in Medicinal Chemistry:
(2E)-N-prop-2-en-1-ylbut-2-enamide is used in medicinal chemistry for its potential biological activities and therapeutic applications, making it a valuable compound for drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 69833-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69833-27:
(7*6)+(6*9)+(5*8)+(4*3)+(3*3)+(2*2)+(1*7)=168
168 % 10 = 8
So 69833-27-8 is a valid CAS Registry Number.

69833-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-N-prop-2-enylbut-2-enamide

1.2 Other means of identification

Product number -
Other names Crotonsaeure-allylamid

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:69833-27-8 SDS

69833-27-8Downstream Products

69833-27-8Relevant academic research and scientific papers

Oxime esters as acylating agents in the aminolysis reaction. A simple and chemoselective method for the preparation of amides from amino alcohols

Fernandez,Menendez,Gotor

, p. 713 - 716 (2007/10/02)

Oxime esters, such as acetone O-alkanoyl-, O-alkenoyl- or O-benzyloxycarbonyloximes, react with amines under extremely mild conditions to give the corresponding amides in very good yield. When amino alcohols are used a total chemoselectivity is observed.

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