(S)-2-((tert-Butoxycarbonyl)amino)-2-(m-tolyl)acetic acid

≥95%

Reagent Code: #38084
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CAS Number 1217677-36-5

science Other reagents with same CAS 1217677-36-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.31 g/mol
Formula C₁₄H₁₉NO₄
badge Registry Numbers
MDL Number MFCD01632531
thermostat Physical Properties
Boiling Point 420.4±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the production of chiral molecules, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex organic syntheses, making it valuable in medicinal chemistry. Additionally, it is utilized in research to study enzyme interactions and receptor binding due to its chiral structure, which mimics natural amino acids. Its applications extend to the development of therapeutic agents for conditions like inflammation, cancer, and metabolic disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,905.00
inventory 1g
10-20 days ฿9,819.00

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(S)-2-((tert-Butoxycarbonyl)amino)-2-(m-tolyl)acetic acid
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This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the production of chiral molecules, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex organic syntheses, making it valuable in medicinal chemistry. Additionally, it is utilized in research to study enzyme interactions and receptor binding due to its chiral

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the production of chiral molecules, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex organic syntheses, making it valuable in medicinal chemistry. Additionally, it is utilized in research to study enzyme interactions and receptor binding due to its chiral structure, which mimics natural amino acids. Its applications extend to the development of therapeutic agents for conditions like inflammation, cancer, and metabolic disorders.

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