190195-77-8

Basic information

• Product Name: 1-((1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-bicyclo[3.1.0]hex-1-yl)-3-((E)-3-methoxy-2-methyl-acryloyl)-urea
• CAS NO: 190195-77-8
• Molecular Weight: 464.561
• Mol File: 190195-77-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-((1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-bicyclo[3.1.0]hex-1-yl)-3-((E)-3-methoxy-2-methyl-acryloyl)-urea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-bicyclo[3.1.0]hex-1-yl)-3-((E)-3-methoxy-2-methyl-acryloyl)-urea(190195-77-8)
• EPA Substance Registry System: 1-((1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-bicyclo[3.1.0]hex-1-yl)-3-((E)-3-methoxy-2-methyl-acryloyl)-urea(190195-77-8)

Safety Data

• Hazardous Substances Data: 190195-77-8(Hazardous Substances Data)

Upstream product

• 170453-01-7 (1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-1-(2-trimethylsilylethoxyformamido)bicyclo<3.1.0>hexane 
• 170452-99-0 (3aR,4R,5S,6aR)-4-Benzyloxymethyl-5-benzyloxy-6a-cyano-3,3a,4,5,6,6a-hexahydrocyclopentapyrazole 
• 190195-74-5 (1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethylbicyclo<3.1.0>hexane-1-carboxylic acid 
• 170453-00-6 (1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-1-cyanobicyclo<3.1.0>hexane 
• 160860-62-8 (1S,2R,3R,4R)-1-Benzyloxy-2-benzyloxymethyl-4-cyano-3-hydroxycyclopentane 
• 170452-98-9 (3R,4S)-1-Cyano-4-benzyloxy-3-benzyloxymethylcyclopentene 
• 110567-22-1 (2R,3S)-benzyloxy-2-benzyloxymethyl-6-oxabicyclo<3.1.0>hexane 
• 52410-41-0 3-methoxy-2-methylacryloyl chloride 
• 132151-65-6 (E)-3-methoxy-2-methylacryloyl isocyanate 
• 170453-02-8 (1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-1-aminobicyclo<3.1.0>hexane 

Downstream Products

• 190195-79-0 (1S,3S,4R,5S)-3-Benzyloxy-4-benzyloxymethyl-1-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)bicyclo<3.1.0>hexane 

Relevant articles and documents

Conformationally locked carbocyclic nucleosides built on a bicyclo[3.1.0]hexane template with a fixed Southern conformation. Synthesis and antiviral activity

The construction of carbocyclic nucleosides with a fixed 3E ring pucker in the Southern hemisphere of the pseudorotational cycle is achieved from a common precursor carbocyclic amine, (1S,3S,4R,5S)-3-benzyloxy-4-benzyloxymethyl-1-aminobicyclo[3