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2-Methylene-beta-alanine, also known as 2-methylen-3-aminopropanoic acid, is an organic compound with the chemical formula C4H7NO2. It is a derivative of beta-alanine, an amino acid that plays a crucial role in the synthesis of carnosine, a dipeptide involved in muscle function and pH buffering. 2-Methylene-beta-alanine is structurally similar to beta-alanine but contains a double bond between the second and third carbon atoms, which gives it unique properties. 2-methylene-beta-alanine has been studied for its potential applications in various fields, including pharmaceuticals and sports nutrition, due to its ability to enhance carnosine levels in muscles, potentially improving exercise performance and reducing muscle fatigue.

4452-16-8

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4452-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4452-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4452-16:
(6*4)+(5*4)+(4*5)+(3*2)+(2*1)+(1*6)=78
78 % 10 = 8
So 4452-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2/c1-3(5)2-4(6)7/h1-2,5H2,(H,6,7)

4452-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-aminobut-3-enoic acid

1.2 Other means of identification

Product number -
Other names ammonio methylacrylate

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:4452-16-8 SDS

4452-16-8Downstream Products

4452-16-8Relevant academic research and scientific papers

Radiochemical 18F-fluoroarylation of unsaturated α-, β- and γ-amino acids, application to a radiolabelled analogue of baclofen

H?fling, Sarah B.,Hultsch, Christina,Wester, Hans-Jürgen,Heinrich, Markus R.

experimental part, p. 11846 - 11851 (2009/04/06)

Unsaturated α-, β- and γ-amino acids have been investigated as substrates for the reductive Meerwein arylation. Radical reactions of this type have been shown to be a valuable tool for the fast and efficient introduction of the 4-[18F]fluorophenyl group into precursor molecules allowing short-time syntheses of potential PET radiotracers, which would be more difficult to access by other methods.

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