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CAS 106391-88-2

:

1,1-Dimethylethyl N-[(1R)-1-formyl-2-methylpropyl]carbamate

Description:
1,1-Dimethylethyl N-[(1R)-1-formyl-2-methylpropyl]carbamate, with the CAS number 106391-88-2, is an organic compound characterized by its carbamate functional group. This substance features a tert-butyl group (1,1-dimethylethyl) attached to a nitrogen atom, which is further linked to a chiral center in the form of a 1-formyl-2-methylpropyl moiety. The presence of the formyl group indicates that it can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The compound is likely to exhibit moderate polarity due to the presence of both hydrophobic tert-butyl and polar carbamate functionalities, influencing its solubility in organic solvents and water. Additionally, the chirality of the molecule may impart specific biological activities or interactions, making it of interest in pharmaceutical applications. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations for its handling and use in chemical processes.
Formula:C10H19NO3
InChI:InChI=1S/C10H19NO3/c1-7(2)8(6-12)11-9(13)14-10(3,4)5/h6-8H,1-5H3,(H,11,13)/t8-/m0/s1
InChI key:InChIKey=YMNBXYLOSIKZGL-QMMMGPOBSA-N
SMILES:[C@@H](NC(OC(C)(C)C)=O)([C@@H](C)C)C=O
Synonyms:
  • 1,1-Dimethylethyl N-[(1R)-1-formyl-2-methylpropyl]carbamate
  • Carbamic acid, (1-formyl-2-methylpropyl)-, 1,1-dimethylethyl ester, (R)-
  • Carbamic acid, [(1R)-1-formyl-2-methylpropyl]-, 1,1-dimethylethyl ester
  • Carbamic acid, N-[(1R)-1-formyl-2-methylpropyl]-, 1,1-dimethylethyl ester
  • tert-Butyl ((R)-3-methyl-1-oxobutan-2-yl)carbamate
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