BOC-D-(2-INDA)GLY-OH, with the CAS number 181227-48-5, is a chemical compound that features a protected amino alcohol structure. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, which is commonly used in peptide synthesis to prevent unwanted reactions. The compound contains a D-configuration of the glycine derivative, indicating its chirality, which is crucial in biological systems. The presence of the indan moiety contributes to its unique properties, potentially influencing its solubility and reactivity. This compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals where specific stereochemistry is essential. Its characteristics may include moderate to high stability under standard conditions, but it may be sensitive to acidic or basic environments due to the presence of the BOC group. Overall, BOC-D-(2-INDA)GLY-OH is significant in research contexts where precise molecular configurations are required for biological activity or therapeutic efficacy.

BOC-D-(2-INDA)GLY-OH

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1H-Indene-2-acetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-dihydro-, (αR)-

(R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-(2,3-DIHYDRO-1H-INDEN-2-YL)ACETIC ACID

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CAS 181227-48-5: BOC-D-(2-INDA)GLY-OH

1H-Indene-2-acetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-dihydro-, (αR)-

Ref: IN-DA0022QY

(R)-2-(TERT-BUTOXYCARBONYLAMINO)-2-(2,3-DIHYDRO-1H-INDEN-2-YL)ACETIC ACID

Ref: 10-F470007

Boc-D-2-indanylgly-OH

Ref: 3D-FB47826