β-L-Ribofuranose 1-Acetate 2,3,5-Tribenzoate

>98.0%(HPLC)

Reagent Code: #59066
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CAS Number 3080-30-6

science Other reagents with same CAS 3080-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 504.49 g/mol
Formula C₂₈H₂₄O₉
badge Registry Numbers
MDL Number MFCD04114304
thermostat Physical Properties
Melting Point 130° C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used extensively in organic synthesis as a protected form of ribose, it serves as a key intermediate in the production of nucleosides and nucleotides. Its benzoate groups provide stability during chemical reactions, allowing selective deprotection for further modifications. This compound is particularly valuable in the synthesis of antiviral and anticancer drugs, where precise control over ribose functionalization is crucial. It also finds application in carbohydrate chemistry research, aiding in the study of glycosylation processes and the development of novel sugar-based therapeutics. Additionally, it is utilized in the preparation of labeled ribose derivatives for biochemical and metabolic studies.

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inventory 1g
10-20 days ฿3,798.00

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β-L-Ribofuranose 1-Acetate 2,3,5-Tribenzoate
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Used extensively in organic synthesis as a protected form of ribose, it serves as a key intermediate in the production of nucleosides and nucleotides. Its benzoate groups provide stability during chemical reactions, allowing selective deprotection for further modifications. This compound is particularly valuable in the synthesis of antiviral and anticancer drugs, where precise control over ribose functionalization is crucial. It also finds application in carbohydrate chemistry research, aiding in the stu

Used extensively in organic synthesis as a protected form of ribose, it serves as a key intermediate in the production of nucleosides and nucleotides. Its benzoate groups provide stability during chemical reactions, allowing selective deprotection for further modifications. This compound is particularly valuable in the synthesis of antiviral and anticancer drugs, where precise control over ribose functionalization is crucial. It also finds application in carbohydrate chemistry research, aiding in the study of glycosylation processes and the development of novel sugar-based therapeutics. Additionally, it is utilized in the preparation of labeled ribose derivatives for biochemical and metabolic studies.

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