(S)-(-)-2-Amino-4-methyl-1,1-diphenyl-1-pentanol

≧95%

Reagent Code: #84881
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CAS Number 78603-97-1

science Other reagents with same CAS 78603-97-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.38 g/mol
Formula C₁₈H₂₃NO
badge Registry Numbers
MDL Number MFCD03093529
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block or intermediate. Its structure makes it valuable in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of drugs that require specific stereochemistry for optimal efficacy. Additionally, it is employed in asymmetric catalysis, aiding in the creation of complex molecules with high enantioselectivity. Researchers also explore its potential in developing novel ligands for metal-catalyzed reactions, which are crucial in fine chemical and pharmaceutical manufacturing. Its unique properties make it a key component in advancing stereoselective synthesis methodologies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿21,591.00
inventory 50mg
10-20 days ฿2,691.00
inventory 250mg
10-20 days ฿8,991.00

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(S)-(-)-2-Amino-4-methyl-1,1-diphenyl-1-pentanol
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This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block or intermediate. Its structure makes it valuable in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of drugs that require specific stereochemistry for optimal efficacy. Additionally, it is employed in asymmetric catalysis, aiding in the creation of complex molecules with high enantioselectivity. Researchers also explore its potential in developing novel

This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block or intermediate. Its structure makes it valuable in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of drugs that require specific stereochemistry for optimal efficacy. Additionally, it is employed in asymmetric catalysis, aiding in the creation of complex molecules with high enantioselectivity. Researchers also explore its potential in developing novel ligands for metal-catalyzed reactions, which are crucial in fine chemical and pharmaceutical manufacturing. Its unique properties make it a key component in advancing stereoselective synthesis methodologies.

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