1453196-48-9

Basic information

• Product Name: (S)-N¹-benzyl-N²-(4-chlorobenzyl)-N²-hydroxypropane-1,2-diamine
• Synonyms: (S)-N¹-benzyl-N²-(4-chlorobenzyl)-N²-hydroxypropane-1,2-diamine
• CAS NO: 1453196-48-9
• Molecular Weight: 304.82
• Mol File: 1453196-48-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-N¹-benzyl-N²-(4-chlorobenzyl)-N²-hydroxypropane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N¹-benzyl-N²-(4-chlorobenzyl)-N²-hydroxypropane-1,2-diamine(1453196-48-9)
• EPA Substance Registry System: (S)-N¹-benzyl-N²-(4-chlorobenzyl)-N²-hydroxypropane-1,2-diamine(1453196-48-9)

Safety Data

• Hazardous Substances Data: 1453196-48-9(Hazardous Substances Data)

Upstream product

• 3848-36-0 4-chlorobenzaldoxime 
• 4383-22-6 Allylbenzylamine 
• 51307-68-7 N-4-chlorobenzylhydroxylamine 

Downstream Products

• 1453196-66-1 (S)-5-benzyl-2-(4-chlorobenzyl)-3-methyl-1,2,5-oxadiazinan-6-one 

Relevant articles and documents

Highly enantioselective intermolecular hydroamination of allylic amines with chiral aldehydes as tethering catalysts

Chirally LinkedIn: Chiral aldehydes are effective tethering catalysts for enantioselective intermolecular hydroamination, which provides access to vicinal diamine motifs in good yields and excellent enantioselectivities (see scheme). This work highlights simple chiral α-oxygenated aldehydes as effective organocatalysts capable of efficiently inducing asymmetry through transient intramolecularity. Copyright