CAS 1468-42-4

6-(carbamoylamino)hexanoic acid

Description:

6-(Carbamoylamino)hexanoic acid, also known by its CAS number 1468-42-4, is an organic compound characterized by the presence of both a carboxylic acid group and an amide functional group. This compound features a hexanoic acid backbone, which consists of a six-carbon chain, with a carbamoylamino group attached at the sixth carbon. The presence of the amide group contributes to its potential as a building block in peptide synthesis and other organic reactions. It is typically a white to off-white solid at room temperature and is soluble in polar solvents due to its functional groups. The compound may exhibit properties such as moderate melting and boiling points, and it can participate in hydrogen bonding, influencing its reactivity and solubility. Its applications may extend to pharmaceuticals, agrochemicals, and biochemical research, particularly in studies involving amino acids and derivatives. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.

Formula: C₇H₁₄N₂O₃

InChI: InChI=1/C7H14N2O3/c8-7(12)9-5-3-1-2-4-6(10)11/h1-5H2,(H,10,11)(H3,8,9,12)

SMILES: C(CCC(=O)O)CCNC(=N)O

Synonyms:

• 6-[(Aminocarbonyl)Amino]Hexanoic Acid
• epsilon-Ureidocaproic acid
• 6-(Carbamoylamino)Hexanoate

6-Ureidohexanoic acid

CAS: 1468-42-4

Formula: C₇H₁₄N₂O₃

Purity: 95%

Molecular weight: 174.1977

Ref: IN-DA001ECS

6-(Carbamoylamino)hexanoic acid

CAS: 1468-42-4

6-(Carbamoylamino)hexanoic acid

Purity: ≥95%

Molecular weight: 174.20g/mol

Ref: 54-OR78316

6-(Carbamoylamino)hexanoic acid

CAS: 1468-42-4

Purity: 95%

Molecular weight: 174.1999969

Ref: 10-F718659

6-(Carbamoylamino)hexanoic acid

CAS: 1468-42-4

6-(Carbamoylamino)hexanoic acid (6ACA) is a synlett that has been shown to be a potent and selective inhibitor of Hsp70. It is functional as a modulator through the interaction with the zinc-binding site, which inhibits ATPase activity. This molecule also acts as a lead molecule for the development of therapeutic agents against various diseases such as cancer, diabetes, and neurodegenerative disorders. The compound has been shown to have catalytic activity in acidic conditions and shows high stereoselectivity in multicomponent reactions.

Formula: C₇H₁₄N₂O₃

Purity: Min. 95%

Molecular weight: 174.2 g/mol

Ref: 3D-BAA46842