(R)-Benzyl but-3-yn-2-ylcarbamate

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Reagent Code: #37763
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CAS Number 1393524-11-2

science Other reagents with same CAS 1393524-11-2

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Weight 203.2371 g/mol
Formula C₁₂H₁₃NO₂
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MDL Number MFCD22548355
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of more complex molecules. Its structure, featuring a carbamate group and an alkyne functionality, makes it a valuable intermediate in the development of pharmaceuticals and bioactive compounds. The chiral center allows for the creation of enantiomerically pure substances, which is crucial in drug development to ensure specificity and efficacy. Additionally, the alkyne group enables further functionalization through reactions such as click chemistry, making it a versatile tool in medicinal chemistry and material science. Its application extends to the synthesis of potential therapeutic agents, including those targeting neurological disorders and cancer, due to its ability to serve as a precursor for biologically active molecules.

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inventory 100mg
10-20 days ฿14,823.00

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(R)-Benzyl but-3-yn-2-ylcarbamate
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of more complex molecules. Its structure, featuring a carbamate group and an alkyne functionality, makes it a valuable intermediate in the development of pharmaceuticals and bioactive compounds. The chiral center allows for the creation of enantiomerically pure substances, which is crucial in drug development to ensure specificity and efficacy. Additionally, the alkyne group

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block for the preparation of more complex molecules. Its structure, featuring a carbamate group and an alkyne functionality, makes it a valuable intermediate in the development of pharmaceuticals and bioactive compounds. The chiral center allows for the creation of enantiomerically pure substances, which is crucial in drug development to ensure specificity and efficacy. Additionally, the alkyne group enables further functionalization through reactions such as click chemistry, making it a versatile tool in medicinal chemistry and material science. Its application extends to the synthesis of potential therapeutic agents, including those targeting neurological disorders and cancer, due to its ability to serve as a precursor for biologically active molecules.

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