tert-Butyl thiophen-3-ylcarbamate

97%

Reagent Code: #148453
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CAS Number 19228-91-2

science Other reagents with same CAS 19228-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.27 g/mol
Formula C₉H₁₃NO₂S
badge Registry Numbers
MDL Number MFCD01928808
thermostat Physical Properties
Melting Point 140°C
Boiling Point 238.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective protection of amines during multi-step reactions, especially where thiophene derivatives are involved. Commonly employed in the development of bioactive molecules due to the thiophene ring’s prevalence in drug-like compounds. Also utilized in the synthesis of functional materials and ligands for catalysis.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Yellow to Tan Powder or Crystals
Purity 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,160.00
inventory 10g
10-20 days ฿4,280.00
inventory 25g
10-20 days ฿10,560.00
tert-Butyl thiophen-3-ylcarbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective protection of amines during multi-step reactions, especially where thiophene derivatives are involved. Commonly employed in the development of bioactive molecules due to the thiophene ring’s prevalence in drug-like compounds. Also utilized in the synthesis of functional materials and ligands for catalysis.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective protection of amines during multi-step reactions, especially where thiophene derivatives are involved. Commonly employed in the development of bioactive molecules due to the thiophene ring’s prevalence in drug-like compounds. Also utilized in the synthesis of functional materials and ligands for catalysis.

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