262852-70-0

Basic information

• Product Name: (2R)-2-amino-4-ethylselanyl-butanoic acid
• Synonyms: (2R)-2-Amino-4-(ethylselanyl)butanoic acid; butanoic acid, 2-amino-4-(ethylseleno)-, (2R)-
• CAS NO: 262852-70-0
• Molecular Formula: C₆H₁₃NO₂Se
• Molecular Weight: 210.13
• Mol File: 262852-70-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 323.9°C at 760 mmHg
• Flash Point: 149.7°C
• Vapor Pressure: 5.16E-05mmHg at 25°C
• CAS DataBase Reference: (2R)-2-amino-4-ethylselanyl-butanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-2-amino-4-ethylselanyl-butanoic acid(262852-70-0)
• EPA Substance Registry System: (2R)-2-amino-4-ethylselanyl-butanoic acid(262852-70-0)

Safety Data

• Hazardous Substances Data: 262852-70-0(Hazardous Substances Data)

Upstream product

• 19635-25-7 (2S)-2-amino-4-(benzylselanyl)butanoic acid 
• 75-03-6 ethyl iodide 
• 74-96-4 ethyl bromide 

Relevant articles and documents

Synthesis of non-natural cofactor analogs of S-adenosyl-L-methionine using methionine adenosyltransferase

The present disclosure relates to the synthesis of non-natural analogs of S-adenosyl-L-methionine (SAM) and/or of Se-adenosyl-L-methionine (SeAM) by reacting a methionine analog and adenosine triphosphate (ATP) in the presence of at least one methionine adenosyltransferase (MAT), and to use thereof with downstream SAM and/or SeAM utilizing enzymes. The non-natural analogs of SAM and/or SeAM have the general formula: where X is S or Se, and R1 is an alkyl group.

Synthesis and application in peptide chemistry of amino acids possessing an optically active selenohomocysteine skeleton.

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