tert-butylN-[(2,4-dimethoxyphenyl)methyl]carbamate

95%

Reagent Code: #220378
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CAS Number 1001181-01-6

science Other reagents with same CAS 1001181-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.32 g/mol
Formula C₁₄H₂₁NO₄
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Storage Room temperature

description Product Description

Used as a protecting group in organic synthesis, particularly for amines. The tert-butyl carbamate (Boc) group stabilizes the amine during reactions sensitive to nitrogen nucleophilicity or basicity. The 2,4-dimethoxybenzyl substituent enhances solubility in organic solvents and allows for selective deprotection under mild oxidative or acidic conditions. Commonly applied in peptide synthesis and pharmaceutical intermediates where stepwise construction and functional group compatibility are critical. Its use enables high yields and purity by minimizing side reactions involving the amine functionality.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,840.00
inventory 100mg
10-20 days ฿4,260.00
inventory 250mg
10-20 days ฿6,000.00
inventory 1g
10-20 days ฿12,070.00
inventory 5g
10-20 days ฿37,660.00

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tert-butylN-[(2,4-dimethoxyphenyl)methyl]carbamate
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Used as a protecting group in organic synthesis, particularly for amines. The tert-butyl carbamate (Boc) group stabilizes the amine during reactions sensitive to nitrogen nucleophilicity or basicity. The 2,4-dimethoxybenzyl substituent enhances solubility in organic solvents and allows for selective deprotection under mild oxidative or acidic conditions. Commonly applied in peptide synthesis and pharmaceutical intermediates where stepwise construction and functional group compatibility are critical. Its

Used as a protecting group in organic synthesis, particularly for amines. The tert-butyl carbamate (Boc) group stabilizes the amine during reactions sensitive to nitrogen nucleophilicity or basicity. The 2,4-dimethoxybenzyl substituent enhances solubility in organic solvents and allows for selective deprotection under mild oxidative or acidic conditions. Commonly applied in peptide synthesis and pharmaceutical intermediates where stepwise construction and functional group compatibility are critical. Its use enables high yields and purity by minimizing side reactions involving the amine functionality.

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