858127-57-8 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
Check Digit Verification of cas no
The CAS Registry Mumber 858127-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,1,2 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 858127-57:
(8*8)+(7*5)+(6*8)+(5*1)+(4*2)+(3*7)+(2*5)+(1*7)=198
198 % 10 = 8
So 858127-57-8 is a valid CAS Registry Number.
858127-57-8Relevant articles and documents
METHOD FOR SYNTHESIZING SAPROPTERIN DIHYDROCHLORIDE
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Paragraph 0038, (2015/03/03)
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
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Paragraph 0056, (2015/04/22)
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.
