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Home  > Ethyl 3-aminobutanoate hydrochloride

AA08015

102014-64-2 | Ethyl 3-aminobutanoate hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $34.00 $24.00 -   +
5g 98% in stock $82.00 $58.00 -   +
10g 98% in stock $131.00 $92.00 -   +
25g 98% in stock $267.00 $187.00 -   +
100g 98% in stock $760.00 $532.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA08015
Chemical Name: Ethyl 3-aminobutanoate hydrochloride
CAS Number: 102014-64-2
Molecular Formula: C6H14ClNO2
Molecular Weight: 167.6339
MDL Number: MFCD22056243
SMILES: CCOC(=O)CC(N)C.Cl

 

Computed Properties
Complexity: 93.1  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • Ethyl 3-aminobutanoate hydrochloride is a valuable compound widely used in chemical synthesis for its versatility and efficacy. This molecule serves as a crucial intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its primary role lies in providing a key building block for the synthesis of complex organic molecules with high yields and purity.In the realm of chemical synthesis, Ethyl 3-aminobutanoate hydrochloride acts as a critical starting material for the creation of biologically active compounds, such as pharmaceuticals and drug candidates. Its presence enables the formation of diverse structural motifs through reactions like acylation, alkylation, and cyclization. This compound's compatibility with a wide range of synthetic methodologies makes it a preferred choice for chemists striving to develop novel compounds with enhanced properties.Moreover, Ethyl 3-aminobutanoate hydrochloride plays a significant role in the synthesis of peptide derivatives and amino acid analogs. As a precursor in peptide coupling reactions, it facilitates the construction of peptide sequences with tailored functionalities and improved biological activities. Its ability to participate in efficient amide bond formation reactions enhances the synthesis of peptide-based drugs and biologically active peptides.Overall, Ethyl 3-aminobutanoate hydrochloride's utility in chemical synthesis extends to various industries, including pharmaceuticals, agrochemicals, and material science. Its strategic importance as a versatile intermediate underscores its value in enabling the efficient and cost-effective production of diverse organic compounds with unique properties and applications.
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