(S)-3-((tert-Butoxycarbonyl)amino)-5-methylhexanoic acid

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Reagent Code: #38383
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CAS Number 132549-43-0

science Other reagents with same CAS 132549-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.32 g/mol
Formula C₁₂H₂₃NO₄
badge Registry Numbers
MDL Number MFCD02101665
thermostat Physical Properties
Boiling Point 374.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used primarily in the synthesis of peptides and pharmaceutical intermediates, this compound serves as a key building block in organic chemistry. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step reactions, making it valuable in the production of complex molecules. It is particularly useful in the development of drugs targeting neurological disorders and metabolic diseases. Additionally, its chiral structure enables the creation of enantiomerically pure compounds, which are critical in drug development for ensuring efficacy and reducing side effects.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,825.00
inventory 100mg
10-20 days ฿801.00
inventory 250mg
10-20 days ฿1,287.00
inventory 5g
10-20 days ฿13,257.00

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(S)-3-((tert-Butoxycarbonyl)amino)-5-methylhexanoic acid
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Used primarily in the synthesis of peptides and pharmaceutical intermediates, this compound serves as a key building block in organic chemistry. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step reactions, making it valuable in the production of complex molecules. It is particularly useful in the development of drugs targeting neurological disorders and metabolic diseases. Additionally, its chiral structure enables the creation of enantiomerically pure compounds, which are critical in drug development for ensuring efficacy and reducing side effects.
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