N1-Boc-4-methyl-1,3-phenylenediamine

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Reagent Code: #87076
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CAS Number 660838-05-1

science Other reagents with same CAS 660838-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.28 g/mol
Formula C₁₂H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD04114554
thermostat Physical Properties
Boiling Point 308.6±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

N1-Boc-4-methyl-1,3-phenylenediamine is a protected intermediate used in organic synthesis, particularly within pharmaceutical research and development. The tert-butoxycarbonyl (Boc) group protects one of the amine functionalities on the 1,3-phenylenediamine core, enabling selective reactions at the unprotected amine or other sites. This compound serves as a building block for synthesizing complex heterocyclic compounds, peptides, and bioactive molecules targeted at various therapeutic applications, such as oncology and neurology. Its methyl substituent at the 4-position provides additional steric and electronic modulation for fine-tuning molecular properties in drug design. Due to its specificity and role in advanced synthetic routes, it is not commonly used in bulk applications like dyes or general materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿6,651.00
250mg
10-20 days ฿2,691.00
5g
10-20 days ฿20,790.00
N1-Boc-4-methyl-1,3-phenylenediamine
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N1-Boc-4-methyl-1,3-phenylenediamine is a protected intermediate used in organic synthesis, particularly within pharmaceutical research and development. The tert-butoxycarbonyl (Boc) group protects one of the amine functionalities on the 1,3-phenylenediamine core, enabling selective reactions at the unprotected amine or other sites. This compound serves as a building block for synthesizing complex heterocyclic compounds, peptides, and bioactive molecules targeted at various therapeutic applications, such

N1-Boc-4-methyl-1,3-phenylenediamine is a protected intermediate used in organic synthesis, particularly within pharmaceutical research and development. The tert-butoxycarbonyl (Boc) group protects one of the amine functionalities on the 1,3-phenylenediamine core, enabling selective reactions at the unprotected amine or other sites. This compound serves as a building block for synthesizing complex heterocyclic compounds, peptides, and bioactive molecules targeted at various therapeutic applications, such as oncology and neurology. Its methyl substituent at the 4-position provides additional steric and electronic modulation for fine-tuning molecular properties in drug design. Due to its specificity and role in advanced synthetic routes, it is not commonly used in bulk applications like dyes or general materials.

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