CAS 16947-89-0

Boc-Dab(Z)-OH . DCHA

Description:

Boc-Dab(Z)-OH.DCHA, with the CAS number 16947-89-0, is a chemical compound that features a protected amino acid structure. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amine, which is commonly used in peptide synthesis to prevent unwanted reactions. The "Dab" refers to 2,4-diaminobutyric acid, indicating the presence of two amino groups in the molecule. The "(Z)" notation signifies that the compound has a specific geometric configuration, typically associated with the double bond in the side chain. The "DCHA" part indicates the presence of a dihydrochloride salt, which can enhance the solubility and stability of the compound in various solvents. This compound is often utilized in the synthesis of peptides and other bioactive molecules due to its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid side chains. Its characteristics make it valuable in pharmaceutical and biochemical research, particularly in the development of therapeutic peptides.

Formula: C₃₀H₅₁N₃O₆

InChI: InChI=1/C12H23N.C10H18N2O6.C8H10/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-10(2,3)18-9(17)12-6(7(13)14)4-5-11-8(15)16;1-2-8-6-4-3-5-7-8/h11-13H,1-10H2;6,11H,4-5H2,1-3H3,(H,12,17)(H,13,14)(H,15,16);3-7H,2H2,1H3/t;6-;/m.0./s1

SMILES: C1CCC(CC1)NC1CCCCC1.CC(C)(C)OC(=N[C@@H](CCNC(=O)O)C(=O)O)O.CCc1ccccc1

Synonyms:

• (2S)-2-(tert-butoxycarbonylamino)-4-(carboxyamino)butanoic acid
• N-cyclohexylcyclohexanamine
• Alpha-Boc-Gamma-Z-(Dl)-Diaminobutyric Acid
• Boc-Dab(Z)-OH・DCHA

Boc-Dab(Z)-OH.DCHA

CAS: 16947-89-0

Formula: C₂₉H₄₇N₃O₆

Purity: 97%

Color and Shape: Solid

Molecular weight: 533.7000

Ref: IN-DA007UVP

Boc-Dab(Z)-OH · DCHA

CAS: 16947-89-0

Boc-Dab(Z)-OH · DCHA

Formula: C₁₇H₂₃N₂O₆·C₁₂H₂₄N

Purity: 97%

Color and Shape: white solid

Molecular weight: 533.70g/mol

Ref: 54-OR36398