858127-57-8

Basic information

• Product Name: 1-Amino-1,5-dideoxy-L-erythro-2-pentulose
• Synonyms: 1-Amino-1,5-dideoxy-L-erythro-2-pentulose;1-Amino-1,5-dideoxy-L-erythro-pentulose;(3S,4S)-1-amino-3,4-dihydroxypentan-2-one
• CAS NO: 858127-57-8
• Molecular Formula: C5H11NO3
• Molecular Weight: 133.14574
• Mol File: 858127-57-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Amino-1,5-dideoxy-L-erythro-2-pentulose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Amino-1,5-dideoxy-L-erythro-2-pentulose(858127-57-8)
• EPA Substance Registry System: 1-Amino-1,5-dideoxy-L-erythro-2-pentulose(858127-57-8)

Safety Data

• Hazardous Substances Data: 858127-57-8(Hazardous Substances Data)

Usage

Chemical Class

Aminosugars

Explanation

1-Amino-1,5-dideoxy-L-erythro-2-pentulose belongs to the class of aminosugars, which are compounds that contain both an amino group and a sugar moiety.

Explanation

It is a derivative of L-erythrulose, which is a ketose sugar, meaning it has a ketone group in its structure.

Explanation

The compound has an amino group (-NH2) and two hydroxyl groups (-OH) attached to its structure, which contribute to its unique properties.

Explanation

1-Amino-1,5-dideoxy-L-erythro-2-pentulose is structurally similar to deoxysugars, which are sugars that have one or more hydroxyl groups replaced by hydrogen atoms.

Explanation

The compound's structure and properties make it a compound of interest for further research in the study of metabolism and biochemical pathways, which could lead to a better understanding of various biological processes.

Explanation

The unique structure and properties of 1-Amino-1,5-dideoxy-L-erythro-2-pentulose make it a compound of interest for potential use in various industries, such as biotechnology, chemical engineering, and materials science.

Derivative of

L-erythrulose

Structural Features

Contains an amino group and two hydroxyl groups

Structural Similarity

Deoxysugars

Potential Applications

Pharmaceutical and drug development

Research Interest

Metabolism and biochemical pathways

Industrial Potential

Various industries

Downstream Products

• 69056-38-8 Sapropterin dihydrochloride 

Relevant articles and documents

METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE

Disclosed is a method for synthesizing sapropterin dihydrochloride. The present invention reduces a synthesis route of the sapropterin dihydrochloride, and resolves a racemate intermediate or an intermediate having a low antimer isomerism value by using a chiral resolving reagent, thereby obtaining an intermediate having a high antimer isomerism value. Raw materials are cheap and readily available, and the cost is significantly reduced, hence providing an effective scheme for mass industrial production of the sapropterin dihydrochloride.

METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE

Disclosed is a method for synthesizing sapropterin dihydrochloride. The present invention reduces a synthesis route of the sapropterin dihydrochloride, introduces a chiral center in an asymmetric synthesis manner, in which a tetrahydrofuran solution containing a samarium catalyst is adopted as a catalyst, and obtains a target compound having a high antimer isomerism value by means of selective catalysis. The yield is improved, raw materials are cheap and readily available, and the cost is significantly reduced, hence providing an effective scheme for mass industrial production of the sapropterin dihydrochloride.

METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE

Disclosed is a method for synthesizing sapropterin dihydrochloride. The present disclosure reduces a synthesis route of the sapropterin dihydrochloride, introduces a chiral center in an asymmetric synthesis manner, in which a tetrahydrofuran solution containing a samarium catalyst is adopted as a catalyst, and obtains a target compound having a high antimer isomerism value by means of selective catalysis. The yield is improved, raw materials are cheap and readily available, and the cost is significantly reduced, hence providing an effective scheme for mass industrial production of the sapropterin dihydrochloride.

METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE

Disclosed is a method for synthesizing sapropterin dihydrochloride. The present disclosure reduces a synthesis route of the sapropterin dihydrochloride, and resolves a racemate intermediate or an intermediate having a low antimer isomerism value by using a chiral resolving reagent, thereby obtaining an intermediate having a high antimer isomerism value. Raw materials are cheap and readily available, and the cost is significantly reduced, hence providing an effective scheme for mass industrial production of the sapropterin dihydrochloride.