FMOC-DL-(Phenyl)gly-OH, with the CAS number 163883-97-4, is a chemical compound commonly used in peptide synthesis and as a protecting group in organic chemistry. The FMOC (9-fluorenylmethoxycarbonyl) group is a widely utilized protective group for amines, allowing for selective reactions without interfering with other functional groups. This compound features a phenyl group attached to a glycine derivative, which contributes to its hydrophobic characteristics and can influence the solubility and reactivity in various solvents. FMOC-DL-(Phenyl)gly-OH is typically a white to off-white solid and is soluble in organic solvents like dichloromethane and dimethylformamide, but less soluble in water. Its stability under basic conditions makes it suitable for use in solid-phase peptide synthesis. Additionally, the presence of both D- and L- configurations in the glycine moiety allows for versatility in synthesizing peptides with specific stereochemical properties. Proper handling and storage are essential, as with many chemical substances, to maintain its integrity and effectiveness in synthetic applications.

FMOC-DL-(PHENYL)GLY-OH

163883-97-4: FMOC-DL-(Phenyl)gly-OH, with the CAS number 163883-97-4, is a chemical compound commonly used in peptide synthesis and as a protecting group in organic chemistry. The FMOC (9-fluorenylmethoxycarbonyl) group is a widely utilized protective group for amines, allowing for selective reactions without interfering with other functional groups. This compound features a phenyl group attached to a glycine derivative, which contributes to its hydrophobic characteristics and can influence the solubility and reactivity in various solvents. FMOC-DL-(Phenyl)gly-OH is typically a white to off-white solid and is soluble in organic solvents like dichloromethane and dimethylformamide, but less soluble in water. Its stability under basic conditions makes it suitable for use in solid-phase peptide synthesis. Additionally, the presence of both D- and L- configurations in the glycine moiety allows for versatility in synthesizing peptides with specific stereochemical properties. Proper handling and storage are essential, as with many chemical substances, to maintain its integrity and effectiveness in synthetic applications.

CAS 163883-97-4

FMOC-DL-(PHENYL)GLY-OH

2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-phenylacetic acid

Ref: IN-DA001UIR

Fmoc-DL-phenylglycine

Ref: 54-OR452093