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28267-25-6

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28267-25-6 Usage

Description

rac-3-AMinoisobutyric Acid Hydrochloride, also known as racemic 3-aminoisobutyric acid hydrochloride, is an organic compound with the chemical formula C4H10NO2·HCl. It is a white crystalline solid and is a derivative of β-alanine, an amino acid that is not coded by genetic code but is a component of coenzyme A and carnitine.

Uses

Used in Pharmaceutical Industry:
rac-3-AMinoisobutyric Acid Hydrochloride is used as an intermediate for the preparation and isolation of D(-)-β-aminoisobutyric acid, which is an important compound in the synthesis of various pharmaceuticals and biologically active molecules. It plays a crucial role in the development of new drugs and therapies.
Used in Chemical Synthesis:
In the field of chemical synthesis, rac-3-AMinoisobutyric Acid Hydrochloride is used as a building block for the creation of various complex organic molecules. Its unique structure allows for the formation of different chemical bonds, making it a versatile compound for synthetic applications.
Used in Research and Development:
rac-3-AMinoisobutyric Acid Hydrochloride is also utilized in research and development for studying the properties and reactivity of β-amino acids. It helps scientists understand the behavior of these compounds in various chemical reactions and their potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 28267-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,6 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28267-25:
(7*2)+(6*8)+(5*2)+(4*6)+(3*7)+(2*2)+(1*5)=126
126 % 10 = 6
So 28267-25-6 is a valid CAS Registry Number.

28267-25-6SDS

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 3-amino-2-methylpropanoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-amino-2-methylpropanoic acid hydrochloride

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:28267-25-6 SDS

28267-25-6Relevant articles and documents

An Efficient Two-Step Preparation of α-, β-, γ- or δ-Amino Acids from 2-Pyrazinones, 2-Hydroxypyrimidines or 2-Pyridones Respectively

Zacharie, Boulos,Abbott, Shaun D.,Baigent, Christopher B.,Doyle, Christopher,Yalagala, Ravi Shekar

, p. 6486 - 6493 (2018/11/23)

A practical and efficient two-step procedure is reported for the preparation of a variety of α-, β-, γ- and δ-amino acids from 2-pyridone, 2-pyrazinone or 2-hydroxypyrimidine and derivatives. The procedure is amenable to scale-up and in most cases no chromatographic purification of the product is required. This approach is useful, especially in the synthesis of amino acids or deuterated amino acids that are not obtained by other methods.

The Stereochemistry of Organometallic Compounds. XXXII. Hydrocyanation of Derivatives of Amino Alkynes

Jackson, W. Roy,Perlmutter, Patrick,Smallridge, Andrew J.

, p. 1201 - 1208 (2007/10/02)

The hydrocyanation of a range of amino alkyne derivatives has been studied by using nickel-based catalyst systems.The phthalimido derivatives have been shown to give good yields of unsaturated cyano amine derivatives, and some of these have been converted into both saturated and unsaturated amino acids.

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