tert-Butyl (tert-butoxycarbonyl)(hydroxy)carbamate

98%

Reagent Code: #151771
fingerprint
CAS Number 142654-29-3

science Other reagents with same CAS 142654-29-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.26 g/mol
Formula C₁₀H₁₉NO₅
badge Registry Numbers
MDL Number MFCD24465969
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a protecting group reagent in organic synthesis, especially in peptide and pharmaceutical manufacturing. It enables selective protection of amine functionalities by forming stable carbamate derivatives that are easily removed under mild acidic conditions. This allows multi-step synthesis to proceed without interference from reactive amine groups. Commonly employed in the production of complex bioactive molecules where precise control over reactivity is required. Also utilized in the development of specialty polymers and agrochemicals due to its reliability in safeguarding functional groups during transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,100.00
inventory 1g
10-20 days ฿9,300.00
inventory 5g
10-20 days ฿34,500.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl (tert-butoxycarbonyl)(hydroxy)carbamate
No image available
Used primarily as a protecting group reagent in organic synthesis, especially in peptide and pharmaceutical manufacturing. It enables selective protection of amine functionalities by forming stable carbamate derivatives that are easily removed under mild acidic conditions. This allows multi-step synthesis to proceed without interference from reactive amine groups. Commonly employed in the production of complex bioactive molecules where precise control over reactivity is required. Also utilized in the develo
Used primarily as a protecting group reagent in organic synthesis, especially in peptide and pharmaceutical manufacturing. It enables selective protection of amine functionalities by forming stable carbamate derivatives that are easily removed under mild acidic conditions. This allows multi-step synthesis to proceed without interference from reactive amine groups. Commonly employed in the production of complex bioactive molecules where precise control over reactivity is required. Also utilized in the development of specialty polymers and agrochemicals due to its reliability in safeguarding functional groups during transformations.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...