Acetyl-O-acetyl-L-threonine

95%

Reagent Code: #137693
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CAS Number 137197-06-9

science Other reagents with same CAS 137197-06-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₈H₁₃NO₅
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex biomolecules where selective deprotection is required. The acetyl group on the hydroxyl side chain prevents unwanted side reactions during coupling steps, making it valuable in solid-phase peptide synthesis. It is also employed in research settings for studying enzyme substrates and metabolic pathways involving threonine modifications. Its stability under various reaction conditions allows for high yields in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿2,380.00
250mg
10-20 days ฿7,740.00
1g
10-20 days ฿23,350.00
5g
10-20 days ฿96,310.00
Acetyl-O-acetyl-L-threonine
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Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex biomolecules where selective deprotection is required. The acetyl group on the hydroxyl side chain prevents unwanted side reactions during coupling steps, making it valuable in solid-phase peptide synthesis. It is also employed in research settings for studying enzyme substrates and metabolic pathways involving threonine modifications. Its stability under various reaction conditions allows for high

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex biomolecules where selective deprotection is required. The acetyl group on the hydroxyl side chain prevents unwanted side reactions during coupling steps, making it valuable in solid-phase peptide synthesis. It is also employed in research settings for studying enzyme substrates and metabolic pathways involving threonine modifications. Its stability under various reaction conditions allows for high yields in multi-step organic syntheses.

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