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CAS 135582-93-3

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Phenylmethyl N-[(2S)-2,3-dihydroxypropyl]carbamate

Description:
Phenylmethyl N-[(2S)-2,3-dihydroxypropyl]carbamate, also known by its CAS number 135582-93-3, is a chemical compound that belongs to the class of carbamates. This substance features a phenylmethyl group attached to a carbamate functional group, which is further linked to a chiral 2,3-dihydroxypropyl moiety. The presence of hydroxyl groups in its structure suggests that it may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. Typically, carbamates are known for their applications in pharmaceuticals and agrochemicals, often serving as intermediates or active ingredients. The stereochemistry of the compound indicates that it may have specific biological activities or interactions, particularly in chiral environments. Its molecular structure suggests potential for various applications, including enzyme inhibition or modulation, making it of interest in medicinal chemistry. As with many organic compounds, its physical properties such as melting point, boiling point, and solubility would depend on the specific conditions and purity of the sample.
Formula:C11H15NO4
InChI:InChI=1S/C11H15NO4/c13-7-10(14)6-12-11(15)16-8-9-4-2-1-3-5-9/h1-5,10,13-14H,6-8H2,(H,12,15)/t10-/m0/s1
InChI key:InChIKey=DAMJAHUBTRVKPI-JTQLQIEISA-N
SMILES:C(OC(NC[C@@H](CO)O)=O)C1=CC=CC=C1
Synonyms:
  • Phenylmethyl N-[(2S)-2,3-dihydroxypropyl]carbamate
  • Carbamic acid, [(2S)-2,3-dihydroxypropyl]-, phenylmethyl ester
  • Carbamic acid, N-[(2S)-2,3-dihydroxypropyl]-, phenylmethyl ester
  • Carbamic acid, (2,3-dihydroxypropyl)-, phenylmethyl ester, (S)-
  • (S)-3-[N-(Benzyloxycarbonyl)amino]-1,2-propanediol
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