606970-33-6

Basic information

• Product Name: (2R,3S,4R,5R,6R)-3,5-Diacetoxy-2-allyl-4-benzyloxy-6-benzyloxymethyl-piperidine-1-carboxylic acid 2,2,2-trichloro-ethyl ester
• Synonyms: (2R,3S,4R,5R,6R)-3,5-Diacetoxy-2-allyl-4-benzyloxy-6-benzyloxymethyl-piperidine-1-carboxylic acid 2,2,2-trichloro-ethyl ester
• CAS NO: 606970-33-6
• Molecular Weight: 642.961
• Mol File: 606970-33-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S,4R,5R,6R)-3,5-Diacetoxy-2-allyl-4-benzyloxy-6-benzyloxymethyl-piperidine-1-carboxylic acid 2,2,2-trichloro-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,4R,5R,6R)-3,5-Diacetoxy-2-allyl-4-benzyloxy-6-benzyloxymethyl-piperidine-1-carboxylic acid 2,2,2-trichloro-ethyl ester(606970-33-6)
• EPA Substance Registry System: (2R,3S,4R,5R,6R)-3,5-Diacetoxy-2-allyl-4-benzyloxy-6-benzyloxymethyl-piperidine-1-carboxylic acid 2,2,2-trichloro-ethyl ester(606970-33-6)

Safety Data

• Hazardous Substances Data: 606970-33-6(Hazardous Substances Data)

Upstream product

• 606970-26-7 Acetic acid (2R,3R,4R,5S,6R)-5-acetoxy-6-allyl-4-benzyloxy-2-benzyloxymethyl-piperidin-3-yl ester 
• 17341-93-4 2,2,2-Trichloroethyl chloroformate 
• 606970-29-0 Acetic acid (2R,3R,4R,5S,6R)-5-acetoxy-6-allyl-4-benzyloxy-2-benzyloxymethyl-1-naphthalen-2-ylmethyl-piperidin-3-yl ester 
• 606970-27-8 [(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-but-3-enyl]-naphthalen-2-ylmethyl-amine 
• 664366-28-3 (2R,3S,4R,5R,6R)-2-Allyl-4-benzyloxy-6-benzyloxymethyl-1-naphthalen-2-ylmethyl-piperidine-3,5-diol 
• 664366-33-0 [1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-meth-(E)-ylidene]-naphthalen-2-ylmethyl-amine 
• 302788-33-6 3,6-di-O-benzyl-4,5-O-isopropylidene-D-xylo-aldehydo-hexos-5-ulo-2,5-furanose 

Downstream Products

• 606970-36-9 (2R,3R,4R,5S,6R)-3,5-Diacetoxy-4-benzyloxy-2-benzyloxymethyl-6-((E)-3-ethoxycarbonyl-allyl)-piperidine-1-carboxylic acid 2,2,2-trichloro-ethyl ester 

Relevant articles and documents

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Cross-metathesis reactions of α-1-C-allyl-1-deoxynojirimycin derivatives 7a,b and various functionalized alkenes mediated by Grubbs's catalyst 3 are reported. The reactions showed reasonable to very good yields and excellent E/Z selectivity. This methodol