669015-46-7

Basic information

• Product Name: Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine
• Synonyms: Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine
• CAS NO: 669015-46-7
• Molecular Weight: 577.764
• Mol File: 669015-46-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine(669015-46-7)
• EPA Substance Registry System: Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-amine(669015-46-7)

Safety Data

• Hazardous Substances Data: 669015-46-7(Hazardous Substances Data)

Upstream product

• 79258-18-7 (2R,3R,4R,5S)-1,3,4,5-tetrakis(benzyloxy)hept-6-en-2-ol 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 110205-68-0 1,3,4,5-tetra-O-benzyl-6,7-dideoxy-L-xylo-hept-6-en-2-ulose 
• 107-11-9 1-amino-2-propene 

Downstream Products

• 669015-47-8 Allyl-((2R,3R,4S)-2,3,4-tris-benzyloxy-1-benzyloxymethyl-hex-5-enyl)-carbamic acid benzyl ester 

Relevant articles and documents

Synthesis and biological evaluation of the first example of an eight-membered iminoalditol

The synthesis of the first examples of eight-membered iminoalditols has been achieved from 2,3,4,6-tetra-O-benzyl-D-glucopyranose by way of a ring-closing metathesis. The (2R,3R,4R,5S)-2-hydroxymethyl-azocane-3,4,5-triol (3a), which has the D-gluco config