CAS 90508-28-4

Aloc-Ala-Oh Dcha

Description:

Aloc-Ala-Oh Dcha, identified by the CAS number 90508-28-4, is a chemical compound that typically functions as a peptide or peptide derivative in various biochemical applications. Its structure includes an alloc-protected alanine residue, which is often utilized in peptide synthesis to facilitate the formation of peptide bonds while preventing unwanted reactions. The presence of the alloc group allows for selective deprotection under specific conditions, making it valuable in synthetic organic chemistry. This compound may be used in the development of pharmaceuticals, particularly in the design of peptide-based drugs or as a building block in combinatorial chemistry. Additionally, its properties may include solubility in organic solvents and stability under standard laboratory conditions, although specific reactivity and stability can vary based on the surrounding environment and the presence of other reagents. As with many chemical substances, handling should be conducted with care, following appropriate safety protocols to mitigate any potential hazards.

Aloc-Ala-OH · DCHA

CAS: 90508-28-4

Bachem ID: 4028865.

Formula: C₇H₁₁NO₄·C₁₂H₂₃N

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 354.49

Ref: 01-4028865

Aloc-Ala-OH

CAS: 90508-28-4

Formula: C₇H₁₁NO₄

Purity: 97%

Color and Shape: Liquid

Molecular weight: 173.1665

Ref: IN-DA00H0EE

(S)-2-(((Allyloxy)carbonyl)amino)propanoic acid

CAS: 90508-28-4

(S)-2-(((Allyloxy)carbonyl)amino)propanoic acid

Purity: 97%

Molecular weight: 173.17g/mol

Ref: 54-OR1056741

(S)-2-(((Allyloxy)carbonyl)amino)propanoic acid

CAS: 90508-28-4

Purity: 97%

Molecular weight: 173.1679993

Ref: 10-F634482

Aloc-Ala-OH·DCHA

CAS: 90508-28-4

Aloc-Ala-OH·DCHA is a linker that can be utilized in nucleotide synthesis. It is synthesized by reacting the amine group of alanine with the acid chloride of DCHA. The product of this reaction, Aloc-Ala-OH·DCHA, is an amide bond with a free hydroxyl group on one end and a free amino group on the other end. The C-terminal carboxylic acid function of this compound reacts with phosphoramidite to yield the desired n-terminal threonine residue. This linker can also be used to conjugate other compounds such as nucleosides or phosphodiester bonds.

Formula: C₇H₁₁NO₄·C₁₂H₂₃N

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 354.48 g/mol

Ref: 3D-FA107861