(1R,2R)-2-methylcyclohexan-1-amine hydrochloride

98%

Reagent Code: #228962
fingerprint
CAS Number 302596-19-6

science Other reagents with same CAS 302596-19-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.66 g/mol
Formula C₇H₁₆ClN
badge Registry Numbers
MDL Number MFCD28978703
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring specific stereochemistry. Its rigid cyclohexyl structure and defined stereochemistry make it valuable for asymmetric synthesis and as a scaffold in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its ability to influence binding selectivity and metabolic stability. Also utilized in the design of catalysts for enantioselective reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿15,260.00
100mg
10-20 days ฿25,930.00
250mg
10-20 days ฿44,080.00
(1R,2R)-2-methylcyclohexan-1-amine hydrochloride
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring specific stereochemistry. Its rigid cyclohexyl structure and defined stereochemistry make it valuable for asymmetric synthesis and as a scaffold in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its ability to influence binding selectivity and metabolic stability. Also utilized in the design of catalysts for ena

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring specific stereochemistry. Its rigid cyclohexyl structure and defined stereochemistry make it valuable for asymmetric synthesis and as a scaffold in medicinal chemistry. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its ability to influence binding selectivity and metabolic stability. Also utilized in the design of catalysts for enantioselective reactions.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...