tert-Butyl (R)-(3-chloro-2-hydroxypropyl)carbamate

98%

Reagent Code: #123647
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CAS Number 1072792-33-6

science Other reagents with same CAS 1072792-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.67 g/mol
Formula C₈H₁₆ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the preparation of chiral intermediates for pharmaceuticals. Its structure, featuring a tert-butyl carbamate group and a chloro-hydroxypropyl moiety, makes it a valuable building block in the development of active pharmaceutical ingredients (APIs). It is often employed in the synthesis of beta-blockers and other cardiovascular drugs, where the chiral center plays a critical role in the drug's efficacy. Additionally, its protective group (tert-butyl carbamate) can be selectively removed under mild conditions, allowing for further functionalization in multi-step synthetic routes. The compound is also used in research for developing novel therapeutic agents due to its versatility and stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,044.00
inventory 1g
10-20 days ฿47,601.00
inventory 100mg
10-20 days ฿12,735.00

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tert-Butyl (R)-(3-chloro-2-hydroxypropyl)carbamate
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This compound is primarily utilized in organic synthesis, particularly in the preparation of chiral intermediates for pharmaceuticals. Its structure, featuring a tert-butyl carbamate group and a chloro-hydroxypropyl moiety, makes it a valuable building block in the development of active pharmaceutical ingredients (APIs). It is often employed in the synthesis of beta-blockers and other cardiovascular drugs, where the chiral center plays a critical role in the drug's efficacy. Additionally, its protective

This compound is primarily utilized in organic synthesis, particularly in the preparation of chiral intermediates for pharmaceuticals. Its structure, featuring a tert-butyl carbamate group and a chloro-hydroxypropyl moiety, makes it a valuable building block in the development of active pharmaceutical ingredients (APIs). It is often employed in the synthesis of beta-blockers and other cardiovascular drugs, where the chiral center plays a critical role in the drug's efficacy. Additionally, its protective group (tert-butyl carbamate) can be selectively removed under mild conditions, allowing for further functionalization in multi-step synthetic routes. The compound is also used in research for developing novel therapeutic agents due to its versatility and stability.

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