Propanol

Application Chiral building block.

( S )-(-)-2-Amino-3-phenyl-1-propanol is a chiral amino alcohol. Application ( S )-(-)-2-Amino-3-phenyl-1-propanol can undergo condensation with 5-nitro­salicylaldehyde to form ( S )-2-[(1-benzyl-2-hydroxy­ethyl­imino)meth­yl]-4-nitro­phenol,

( S )-(-)-2-Amino-3-phenyl-1-propanol is a chiral amino alcohol. Application ( S )-(-)-2-Amino-3-phenyl-1-propanol can undergo condensation with 5-nitro­salicylaldehyde to form ( S )-2-[(1-benzyl-2-hydroxy­ethyl­imino)meth­yl]-4-nitro­phenol,

(S)-2-(Boc-amino)-1-propanol

Analysis Note Assay (GC, area%): &#8805 96.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Analysis Note Assay (GC, area%): &#8805 96.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Application 1,3-Diamino-2-propanol was used in the synthesis of poly(2-hydroxypropylene imine), poly(2-hydroxypropylene imine ethylene imine) and poly(hydroxypropylene imine propylene imine). It was also used in the synthesis of tetranuclear mixed

Application 1,3-Diamino-2-propanol was used in the synthesis of poly(2-hydroxypropylene imine), poly(2-hydroxypropylene imine ethylene imine) and poly(hydroxypropylene imine propylene imine). It was also used in the synthesis of tetranuclear mixed

Application 1,3-Diamino-2-propanol is a versatile bidentate diamine ligand which is used in the synthesis of a variety of organometallic compounds. It is a precursor to synthesize the fluorogenic dsDNA binder, N 1 , N 3

Application 1,3-Diamino-2-propanol is a versatile bidentate diamine ligand which is used in the synthesis of a variety of organometallic compounds. It is a precursor to synthesize the fluorogenic dsDNA binder, N 1 , N 3

1,3-Dichloro-2-propanol is a food processing contaminant . Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated .

1,3-Dichloro-2-propanol is a food processing contaminant . Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated .