tert-Butyl 2-chloro-1H-benzo[d]imidazole-1-carboxylate

≥95%

Reagent Code: #148270
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CAS Number 214147-60-1

science Other reagents with same CAS 214147-60-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.70 g/mol
Formula C₁₂H₁₃ClN₂O₂
badge Registry Numbers
MDL Number MFCD21099394
thermostat Physical Properties
Boiling Point 367.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as an intermediate and protecting group in the synthesis of pharmaceuticals, particularly in the development of antiviral, antifungal, and anticancer agents. The tert-butyl carboxylate moiety acts as a Boc protecting group for the imidazole nitrogen, which can be selectively removed under mild acidic conditions, facilitating multi-step organic syntheses. Its structure enables precise modifications in drug design, enhancing metabolic stability, bioavailability, and specificity of active compounds. Commonly employed in research for constructing benzimidazole-based scaffolds, which are key in medicinal chemistry due to their biological activity. Also utilized in the preparation of kinase inhibitors and other targeted therapies in oncology.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,390.00
inventory 5g
10-20 days ฿6,860.00

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tert-Butyl 2-chloro-1H-benzo[d]imidazole-1-carboxylate
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Used as an intermediate and protecting group in the synthesis of pharmaceuticals, particularly in the development of antiviral, antifungal, and anticancer agents. The tert-butyl carboxylate moiety acts as a Boc protecting group for the imidazole nitrogen, which can be selectively removed under mild acidic conditions, facilitating multi-step organic syntheses. Its structure enables precise modifications in drug design, enhancing metabolic stability, bioavailability, and specificity of active compounds. Co

Used as an intermediate and protecting group in the synthesis of pharmaceuticals, particularly in the development of antiviral, antifungal, and anticancer agents. The tert-butyl carboxylate moiety acts as a Boc protecting group for the imidazole nitrogen, which can be selectively removed under mild acidic conditions, facilitating multi-step organic syntheses. Its structure enables precise modifications in drug design, enhancing metabolic stability, bioavailability, and specificity of active compounds. Commonly employed in research for constructing benzimidazole-based scaffolds, which are key in medicinal chemistry due to their biological activity. Also utilized in the preparation of kinase inhibitors and other targeted therapies in oncology.

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