Carbamic acid, N-(1,1-dioxido-3-thietanyl)-, 1,1-dimethylethyl ester

≥95%

Reagent Code: #159404
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Alias 3-(BOC-amino)cyclopropane-1,1-dioxide
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CAS Number 1332628-90-6

science Other reagents with same CAS 1332628-90-6

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Weight 221.27 g/mol
Formula C₈H₁₅NO₄S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-lactamase inhibitors. It plays a key role in constructing protected carbamate derivatives that are essential in multi-step organic syntheses. Its structure allows for selective deprotection and functionalization, making it valuable in medicinal chemistry for modifying amine-containing compounds. Commonly employed in the preparation of antibiotics where controlled amine reactivity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,040.00
inventory 250mg
10-20 days ฿4,870.00
inventory 1g
10-20 days ฿19,010.00

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Carbamic acid, N-(1,1-dioxido-3-thietanyl)-, 1,1-dimethylethyl ester
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-lactamase inhibitors. It plays a key role in constructing protected carbamate derivatives that are essential in multi-step organic syntheses. Its structure allows for selective deprotection and functionalization, making it valuable in medicinal chemistry for modifying amine-containing compounds. Commonly employed in the preparation of antibiotics where controlled amine reactivity is required.

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of beta-lactamase inhibitors. It plays a key role in constructing protected carbamate derivatives that are essential in multi-step organic syntheses. Its structure allows for selective deprotection and functionalization, making it valuable in medicinal chemistry for modifying amine-containing compounds. Commonly employed in the preparation of antibiotics where controlled amine reactivity is required.

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