(R)-1, 1-Bis(4-methoxyphenyl)-3-methylbutane-1, 2-diamine

98%

Reagent Code: #231074
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CAS Number 166764-19-8

science Other reagents with same CAS 166764-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.42 g/mol
Formula C₁₉H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD02684539
thermostat Physical Properties
Melting Point 78-98 °C
Boiling Point 477.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof

description Product Description

Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in the development of pharmaceuticals. Its structural features enable high enantioselectivity in catalytic reactions, making it valuable in the production of optically active drugs. Commonly applied in the synthesis of bioactive molecules where stereochemistry plays a critical role in biological activity. Also utilized in research settings for the preparation of chiral amines and amine derivatives through reductive amination and other carbon–nitrogen bond-forming reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,570.00
1g
10-20 days ฿3,670.00
5g
10-20 days ฿17,810.00
25g
10-20 days ฿83,370.00
(R)-1, 1-Bis(4-methoxyphenyl)-3-methylbutane-1, 2-diamine
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Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in the development of pharmaceuticals. Its structural features enable high enantioselectivity in catalytic reactions, making it valuable in the production of optically active drugs. Commonly applied in the synthesis of bioactive molecules where stereochemistry plays a critical role in biological activity. Also utilized in research settings for the preparation of chiral amines and amine derivatives through reductive amination an

Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in the development of pharmaceuticals. Its structural features enable high enantioselectivity in catalytic reactions, making it valuable in the production of optically active drugs. Commonly applied in the synthesis of bioactive molecules where stereochemistry plays a critical role in biological activity. Also utilized in research settings for the preparation of chiral amines and amine derivatives through reductive amination and other carbon–nitrogen bond-forming reactions.

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