Boc-D-Glu(Ome)-OH.DCHA

≥95%

Reagent Code: #50254
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CAS Number 76379-02-7

science Other reagents with same CAS 76379-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 442.59 g/mol
Formula C₂₃H₄₂N₂O₆
badge Registry Numbers
MDL Number MFCD01861340
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used extensively in peptide synthesis, this compound is a protected form of D-glutamic acid, with the α-amino group protected by Boc (tert-butoxycarbonyl), the side-chain γ-carboxylic acid as methyl ester (OMe), and the α-carboxylic acid as DCHA (dicyclohexylamine) salt. This ensures selective reactions during the assembly of peptide chains. The Boc group provides stability under various conditions, while the DCHA salt enhances solubility and handling. Commonly applied in the production of pharmaceuticals and bioactive peptides, especially in solid-phase synthesis, it plays a crucial role in the development of drugs targeting neurological disorders, cancer, and metabolic diseases. Additionally, it is utilized in research to study enzyme mechanisms and protein interactions due to its ability to maintain structural integrity during complex reactions.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,332.00
inventory 1g
10-20 days ฿414.00
inventory 10g
10-20 days ฿2,070.00

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Boc-D-Glu(Ome)-OH.DCHA
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Used extensively in peptide synthesis, this compound is a protected form of D-glutamic acid, with the α-amino group protected by Boc (tert-butoxycarbonyl), the side-chain γ-carboxylic acid as methyl ester (OMe), and the α-carboxylic acid as DCHA (dicyclohexylamine) salt. This ensures selective reactions during the assembly of peptide chains. The Boc group provides stability under various conditions, while the DCHA salt enhances solubility and handling. Commonly applied in the production

Used extensively in peptide synthesis, this compound is a protected form of D-glutamic acid, with the α-amino group protected by Boc (tert-butoxycarbonyl), the side-chain γ-carboxylic acid as methyl ester (OMe), and the α-carboxylic acid as DCHA (dicyclohexylamine) salt. This ensures selective reactions during the assembly of peptide chains. The Boc group provides stability under various conditions, while the DCHA salt enhances solubility and handling. Commonly applied in the production of pharmaceuticals and bioactive peptides, especially in solid-phase synthesis, it plays a crucial role in the development of drugs targeting neurological disorders, cancer, and metabolic diseases. Additionally, it is utilized in research to study enzyme mechanisms and protein interactions due to its ability to maintain structural integrity during complex reactions.

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