A 410099.1, amine-Boc hydrochloride

98%

Reagent Code: #107440
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CAS Number 2374122-37-7

science Other reagents with same CAS 2374122-37-7

blur_circular Chemical Specifications

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Weight 620.22 g/mol
Formula C₃₂H₅₀ClN₅O₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This product is an amine protected with the Boc (tert-butoxycarbonyl) group in its hydrochloride salt form. It serves as a key intermediate in organic synthesis, particularly in the production of peptides, pharmaceuticals, and agrochemicals. The Boc protection shields the amine functionality, allowing selective reactions on other parts of the molecule without interference. The protecting group can be readily removed under mild acidic conditions to afford the free amine hydrochloride. The hydrochloride salt form improves solubility in aqueous media, facilitating its use in various synthetic protocols. This compound is essential in multi-step processes requiring precise control over reactivity and orthogonal protection strategies.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿23,040.00
inventory 5mg
10-20 days ฿66,240.00

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A 410099.1, amine-Boc hydrochloride
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This product is an amine protected with the Boc (tert-butoxycarbonyl) group in its hydrochloride salt form. It serves as a key intermediate in organic synthesis, particularly in the production of peptides, pharmaceuticals, and agrochemicals. The Boc protection shields the amine functionality, allowing selective reactions on other parts of the molecule without interference. The protecting group can be readily removed under mild acidic conditions to afford the free amine hydrochloride. The hydrochloride sa

This product is an amine protected with the Boc (tert-butoxycarbonyl) group in its hydrochloride salt form. It serves as a key intermediate in organic synthesis, particularly in the production of peptides, pharmaceuticals, and agrochemicals. The Boc protection shields the amine functionality, allowing selective reactions on other parts of the molecule without interference. The protecting group can be readily removed under mild acidic conditions to afford the free amine hydrochloride. The hydrochloride salt form improves solubility in aqueous media, facilitating its use in various synthetic protocols. This compound is essential in multi-step processes requiring precise control over reactivity and orthogonal protection strategies.

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