Boc-D-Glu(ochex)-OH
97%
Reagent
Code: #104696
Alias
BOC-D-GLUTAMIC ACID(OCHEX)-OH;N-[(1,1-Dimethylethoxy)Carbonyl]-D-Glutamic Acid 5-Cyclohexyl Ester;BOC-D-GLUTAMIC ACID Y-CYCLOHEXYLESTER
CAS Number
133464-27-4
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
329.40 g/mol
Formula
C₁₆H₂₇NO₆
badge
Registry Numbers
MDL Number
MFCD00076929
thermostat
Physical Properties
Boiling Point
502.6±45.0 °C at 760 mmHg
inventory_2
Storage & Handling
Density
1.2±0.1 g/cm3
Storage
2-8°C, sealed, dry
description Product Description
This compound is primarily used in peptide synthesis as a protected form of glutamic acid. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amino functionality, while the OChex (cyclohexyl ester) group protects the carboxylic acid side chain of glutamic acid. This protection is crucial during the stepwise assembly of peptides to prevent unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are required to build the peptide chain. The compound ensures the precise incorporation of glutamic acid into the desired peptide sequence, making it essential in the development of pharmaceuticals, bioactive peptides, and research applications involving peptide-based studies.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Solid |
Purity (%) | 96.5-100 |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
shopping_cart Available Sizes & Pricing
Boc-D-Glu(ochex)-OH
This compound is primarily used in peptide synthesis as a protected form of glutamic acid. The Boc (tert-butoxycarbonyl) group serves as a protective group for the amino functionality, while the OChex (cyclohexyl ester) group protects the carboxylic acid side chain of glutamic acid. This protection is crucial during the stepwise assembly of peptides to prevent unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are required to build the peptide chain. The compound ensures the precise incorporation of glutamic acid into the desired peptide sequence, making it essential in the development of pharmaceuticals, bioactive peptides, and research applications involving peptide-based studies.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
฿0.00
Total
฿0.00
THB