tert-Butyl (4-methoxyphenyl)carbamate

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Reagent Code: #149831
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CAS Number 18437-68-8

science Other reagents with same CAS 18437-68-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.27 g/mol
Formula C₁₂H₁₇NO₃
badge Registry Numbers
MDL Number MFCD00816766
thermostat Physical Properties
Boiling Point 278.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a protecting group reagent in organic synthesis, particularly in peptide and pharmaceutical manufacturing. The tert-butyl carbamate (Boc) group stabilizes amines during reactions, preventing unwanted side reactions. The 4-methoxyphenyl variant enhances solubility and crystallinity, aiding in intermediate isolation. Commonly applied in the synthesis of complex molecules where selective deprotection and mild reaction conditions are required. Also utilized in the development of agrochemicals and active pharmaceutical ingredients (APIs) due to its stability under a range of reaction conditions and ease of removal under acidic conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿760.00
inventory 25g
10-20 days ฿3,590.00
inventory 100g
10-20 days ฿13,970.00

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tert-Butyl (4-methoxyphenyl)carbamate
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Used as a protecting group reagent in organic synthesis, particularly in peptide and pharmaceutical manufacturing. The tert-butyl carbamate (Boc) group stabilizes amines during reactions, preventing unwanted side reactions. The 4-methoxyphenyl variant enhances solubility and crystallinity, aiding in intermediate isolation. Commonly applied in the synthesis of complex molecules where selective deprotection and mild reaction conditions are required. Also utilized in the development of agrochemicals and act

Used as a protecting group reagent in organic synthesis, particularly in peptide and pharmaceutical manufacturing. The tert-butyl carbamate (Boc) group stabilizes amines during reactions, preventing unwanted side reactions. The 4-methoxyphenyl variant enhances solubility and crystallinity, aiding in intermediate isolation. Commonly applied in the synthesis of complex molecules where selective deprotection and mild reaction conditions are required. Also utilized in the development of agrochemicals and active pharmaceutical ingredients (APIs) due to its stability under a range of reaction conditions and ease of removal under acidic conditions.

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