Description

5-[3-Buten-1-Yl[(Phenylmethoxy)Carbonyl]Amino]-1,2,5-Trideoxy-D-Erythro-Pent-1-Enitol is a sophisticated chiral building block and protected amino sugar derivative, essential for advanced organic synthesis. This compound is valued for its role in constructing complex molecular architectures, particularly in the development of novel pharmaceuticals and bioactive molecules. It is primarily targeted at research institutions and pharmaceutical companies engaged in carbohydrate chemistry, medicinal chemistry, and the synthesis of nucleoside analogs or glycosidase inhibitors.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new active pharmaceutical ingredients (APIs), especially in antiviral and anticancer drug candidates.
• Carbohydrate Chemistry Research: Serves as a protected precursor for the synthesis of complex oligosaccharides, glycoconjugates, and modified sugars.
• Nucleoside Analog Synthesis: Used in the preparation of novel nucleoside derivatives for potential use as therapeutics or biochemical probes.
• Medicinal Chemistry & Library Synthesis: Employed in high-throughput screening and combinatorial chemistry to generate diverse compound libraries for biological evaluation.
• Biochemical Tool Development: Acts as a substrate or inhibitor in enzymatic studies, particularly those involving glycosidases or glycosyltransferases.
• Academic & Industrial R&D: A critical reagent for method development and exploratory synthesis in organic and bioorganic chemistry laboratories.

Basic Information

Product Name	5-[3-Buten-1-Yl[(Phenylmethoxy)Carbonyl]Amino]-1,2,5-Trideoxy-D-Erythro-Pent-1-Enitol
CAS No.	1315552-00-1
Molecular Formula	C17H23NO5
Molecular Weight	321.37 g/mol
Synonyms	1,2,5-Trideoxy-5-[[(phenylmethoxy)carbonyl][3-buten-1-yl]amino]-D-erythro-pent-1-enitol; (2R,3S)-1-[(Benzyloxy)carbonyl(but-3-en-1-yl)amino]-3,4-dihydroxybut-1-en-2-ol; Cbz-Protected Butenylamino Pentenitol Derivative; D-Erythro-Pentenitol Cbz-Butenylamine; Advanced Chiral Amino Sugar Building Block
EINECS	Contact for details

Quality Control

Our production of this high-value chemical intermediate adheres to stringent quality protocols to ensure batch-to-batch consistency and purity. Each lot is characterized using advanced analytical techniques including HPLC, NMR, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment, supporting your critical R&D and cGMP-compliant development work.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The compound is light-sensitive; prolonged exposure to light should be avoided. Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Specific Rotation	Contact for details
Water Content (KF)	≤ 0.5%
Residual Solvents (GC)	Meets ICH guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.