103023-51-4 | trans-4-(Dimethylamino)cyclohexanol

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$74.00	$52.00
1g	95%	in stock	$216.00	$151.00
5g	95%	in stock	$761.00	$533.00
25g	95%	in stock	$2,623.00	$1,836.00
100g	95%	in stock	$7,752.00	$5,427.00

Description

• Catalog Number: AE10409
• Chemical Name: trans-4-(Dimethylamino)cyclohexanol
• CAS Number: 103023-51-4
• Molecular Formula: C8H17NO
• Molecular Weight: 143.2267
• MDL Number: MFCD09258736
• SMILES: O[C@@H]1CC[C@H](CC1)N(C)C

Computed Properties

• Complexity: 95.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.9

Upstream Synthesis Route

Trans-4-(Dimethylamino)cyclohexanol, also known as DMACH, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable reagent in various organic transformations. DMACH is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its functionality as a chiral building block and its ability to promote selective reactions. In particular, DMACH serves as an effective chiral auxiliary in asymmetric synthesis, enabling the stereochemical control of key intermediates. Additionally, DMACH can participate in C-C bond formation reactions, such as Mannich and Michael additions, leading to the creation of complex molecular structures with high efficiency. Its compatibility with a wide range of functional groups further enhances its utility in organic synthesis, making it a favored choice for chemists seeking to introduce both stereochemical and structural diversity in their target molecules. By incorporating DMACH into synthetic pathways, chemists can access novel compounds with diverse biological activities and potential applications in various industries.