1141934-97-5 | Benzenemethanol, α-(2-aminoethyl)-3-(cyclohexylmethoxy)-, hydrochloride (1:1), (αR)-

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	in stock	$105.00	$73.00
10mg	95%	in stock	$202.00	$141.00
25mg	95%	in stock	$328.00	$229.00
50mg	95%	in stock	$538.00	$376.00

Description

• Catalog Number: AA13751
• Chemical Name: Benzenemethanol, α-(2-aminoethyl)-3-(cyclohexylmethoxy)-, hydrochloride (1:1), (αR)-
• CAS Number: 1141934-97-5
• Molecular Formula: C16H26ClNO2
• Molecular Weight: 299.8361
• MDL Number: MFCD28400873
• SMILES: NCC[C@H](c1cccc(c1)OCC1CCCCC1)O.Cl

Upstream Synthesis Route

The application of (1R)-3-amino-1-[3-(cyclohexylmethoxy)phenyl]propan-1-ol hydrochloride in chemical synthesis is significant in various reactions and processes within the field of organic chemistry. This compound serves as a valuable building block in the synthesis of complex molecules and pharmaceutical intermediates. Its asymmetric nature, due to the presence of the chiral center, makes it particularly useful in producing enantiomerically pure compounds.In chemical synthesis, (1R)-3-amino-1-[3-(cyclohexylmethoxy)phenyl]propan-1-ol hydrochloride can be utilized as a key starting material for the creation of structurally diverse compounds through various synthetic strategies such as asymmetric synthesis, cross-coupling reactions, and functional group transformations. Its unique structure containing an amino group, a substituted phenyl ring, and a cyclohexylmethoxy moiety allows for versatile reactivity and selective functionalization, enabling access to a wide range of chemical entities with specific properties and biological activities.Moreover, the hydrochloride salt form of (1R)-3-amino-1-[3-(cyclohexylmethoxy)phenyl]propan-1-ol offers enhanced stability and solubility, making it easier to handle and manipulate in synthetic procedures. Its presence in asymmetric catalysis and as a chiral auxiliary has also been explored, showcasing its utility in facilitating stereocontrolled reactions and enabling the synthesis of enantiomerically enriched compounds.Overall, the application of (1R)-3-amino-1-[3-(cyclohexylmethoxy)phenyl]propan-1-ol hydrochloride in chemical synthesis provides chemists with a versatile and valuable tool for constructing complex organic molecules with high levels of structural and stereochemical control, driving advancements in the development of novel materials, pharmaceuticals, and biologically active compounds.