(R)-()-2-Amino-3-methyl-1,1-diphenyl-1-butanol

98%

  • Product Code: 59241
  CAS:    86695-06-9
Molecular Weight: 255.35 g./mol Molecular Formula: C₁₇H₂₁NO
EC Number: MDL Number: MFCD01318247
Melting Point: 95-99°C (Lit.) Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: (R)-()-2-Amino-3-methyl-1,1-diphenyl-1-butanol is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block in the development of various biologically active compounds, particularly in the synthesis of enantiomerically pure drugs. Its structure is valuable in asymmetric synthesis, where it acts as a ligand or catalyst to induce chirality in target molecules, enhancing the efficacy and specificity of pharmaceutical agents. Additionally, it is explored in the study of receptor-ligand interactions and the development of central nervous system (CNS) drugs due to its potential to interact with neurotransmitter systems. Its unique stereochemistry also makes it a candidate for research in materials science, particularly in the design of chiral polymers or catalysts.
Product Specification:
Test Specification
Purity 97.5-100%
Melting point 96-100
Specific Rotation (20°C, CHCl3) 140-144
Appearance White to very pale yellow, crystal to powder
Sizes / Availability / Pricing:
Size Availability Price Quantity
1.000 G 10-20 days ฿2,178.00
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5.000 G 10-20 days ฿8,811.00
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(R)-()-2-Amino-3-methyl-1,1-diphenyl-1-butanol
(R)-()-2-Amino-3-methyl-1,1-diphenyl-1-butanol is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a chiral building block in the development of various biologically active compounds, particularly in the synthesis of enantiomerically pure drugs. Its structure is valuable in asymmetric synthesis, where it acts as a ligand or catalyst to induce chirality in target molecules, enhancing the efficacy and specificity of pharmaceutical agents. Additionally, it is explored in the study of receptor-ligand interactions and the development of central nervous system (CNS) drugs due to its potential to interact with neurotransmitter systems. Its unique stereochemistry also makes it a candidate for research in materials science, particularly in the design of chiral polymers or catalysts.
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