H-Ala-Ala-OtBu·HCl, also known as N-tert-butoxycarbonyl (Boc) di-alanine hydrochloride, is a protected form of the dipeptide composed of two alanine residues. This compound is characterized by its stability and solubility in polar solvents, making it suitable for various synthetic applications in peptide chemistry. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the peptide bond formation. The presence of hydrochloride indicates that the compound is in its salt form, enhancing its solubility in aqueous environments. H-Ala-Ala-OtBu·HCl is often utilized in peptide synthesis, particularly in solid-phase synthesis, where the protection and deprotection of amino acids are crucial steps. Its molecular structure includes two alanine units linked by a peptide bond, contributing to its biological relevance in protein synthesis and function. Overall, this compound is significant in the field of organic and medicinal chemistry, particularly in the development of peptide-based therapeutics.

H-Ala-Ala-OtBu . HCl

60417-38-1: H-Ala-Ala-OtBu·HCl, also known as N-tert-butoxycarbonyl (Boc) di-alanine hydrochloride, is a protected form of the dipeptide composed of two alanine residues. This compound is characterized by its stability and solubility in polar solvents, making it suitable for various synthetic applications in peptide chemistry. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amino functionality, allowing for selective reactions without interfering with the peptide bond formation. The presence of hydrochloride indicates that the compound is in its salt form, enhancing its solubility in aqueous environments. H-Ala-Ala-OtBu·HCl is often utilized in peptide synthesis, particularly in solid-phase synthesis, where the protection and deprotection of amino acids are crucial steps. Its molecular structure includes two alanine units linked by a peptide bond, contributing to its biological relevance in protein synthesis and function. Overall, this compound is significant in the field of organic and medicinal chemistry, particularly in the development of peptide-based therapeutics.

H-Ala-Ala-OtBu · HCl

H-Ala-Ala-OBtu hydrochloride

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CAS 60417-38-1

H-Ala-Ala-OtBu . HCl

H-Ala-Ala-OtBu · HCl

Ref: 01-4013847

H-Ala-Ala-OBtu hydrochloride

Ref: 7W-GM6932

H-Ala-Ala-OtBu·HCl

Ref: 3D-FA108274