(S)-2-(2-Chlorophenyl)pyrrolidine

95%

Reagent Code: #38127
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CAS Number 1217788-99-2

science Other reagents with same CAS 1217788-99-2

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Weight 181.6620 g/mol
Formula C₁₀H₁₂ClN
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MDL Number MFCD06762561
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description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly as a chiral building block for the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a chlorophenyl group, makes it a valuable intermediate in the creation of compounds targeting neurological disorders, such as antidepressants and antipsychotics. Additionally, it is employed in the study of receptor-ligand interactions, aiding in the design of drugs with improved selectivity and efficacy. Its chiral nature also allows for the exploration of stereochemistry in drug design, enhancing the understanding of how different enantiomers interact with biological systems.

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inventory 100mg
10-20 days ฿11,790.00

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(S)-2-(2-Chlorophenyl)pyrrolidine
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly as a chiral building block for the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a chlorophenyl group, makes it a valuable intermediate in the creation of compounds targeting neurological disorders, such as antidepressants and antipsychotics. Additionally, it is employed in the study of receptor-ligand interactions, aiding in the design of drugs with improv

This compound is primarily utilized in the field of pharmaceutical research and development, particularly as a chiral building block for the synthesis of various bioactive molecules. Its structure, featuring a pyrrolidine ring and a chlorophenyl group, makes it a valuable intermediate in the creation of compounds targeting neurological disorders, such as antidepressants and antipsychotics. Additionally, it is employed in the study of receptor-ligand interactions, aiding in the design of drugs with improved selectivity and efficacy. Its chiral nature also allows for the exploration of stereochemistry in drug design, enhancing the understanding of how different enantiomers interact with biological systems.

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