1005001-53-5

Basic information

• Product Name: (2S,3S)-(2-N-(p-phenylazo)benzamido)-1,3-dihydroxybutane
• Synonyms: (2S,3S)-(2-N-(p-phenylazo)benzamido)-1,3-dihydroxybutane
• CAS NO: 1005001-53-5
• Molecular Weight: 313.356
• Mol File: 1005001-53-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3S)-(2-N-(p-phenylazo)benzamido)-1,3-dihydroxybutane(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-(2-N-(p-phenylazo)benzamido)-1,3-dihydroxybutane(1005001-53-5)
• EPA Substance Registry System: (2S,3S)-(2-N-(p-phenylazo)benzamido)-1,3-dihydroxybutane(1005001-53-5)

Safety Data

• Hazardous Substances Data: 1005001-53-5(Hazardous Substances Data)

Upstream product

• 150-13-0 4-amino-benzoic acid 
• 98-95-3 nitrobenzene 
• 115584-73-1 p-phenylazobenzoic acid N-hydroxysuccinimidyl ester 
• 44520-55-0 D-threoninol 

Downstream Products

• 1266659-38-4 C₃₈H₃₇N₃O₅ 

Relevant articles and documents

Structural stability of the photo-responsive DNA duplexes containing one azobenzene: Via a confined pore

Herein, the structural stability of single azobenzene modified DNA duplexes, including the trans form and cis form, has been examined separately based on their distinguishable unzipping kinetics from the mixture by an α-hemolysin nanopore. Furthermore, the accurate isomerization efficiency between the trans and cis form was obtained with single molecule resolution.

Synthesis of nucleoside analogues in a ball mill: Fast, chemoselective and high yielding acylation without undesirable solvents

The chemoselective acylation of primary aliphatic amines has been achieved in under ten minutes (and for aromatic amines under 120 min) using vibration ball-milling, avoiding undesirable solvents which are typically employed for such reactions (e.g. DMF).