1170670-30-0

Basic information

• Product Name: methyl 3-C-allyl-2-N-(N-benzylacrylamido)-(R)-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside
• Synonyms: methyl 3-C-allyl-2-N-(N-benzylacrylamido)-(R)-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside
• CAS NO: 1170670-30-0
• Molecular Weight: 449.547
• Mol File: 1170670-30-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 3-C-allyl-2-N-(N-benzylacrylamido)-(R)-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-C-allyl-2-N-(N-benzylacrylamido)-(R)-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside(1170670-30-0)
• EPA Substance Registry System: methyl 3-C-allyl-2-N-(N-benzylacrylamido)-(R)-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside(1170670-30-0)

Safety Data

• Hazardous Substances Data: 1170670-30-0(Hazardous Substances Data)

Upstream product

• 1170670-29-7 methyl 3-C-allyl-2-benzylamino-(R)-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside 
• 814-68-6 acryloyl chloride 

Downstream Products

• 1170670-31-1 methyl 2-benzylamino-(R)-4,6-O-benzylidene-2-N,3-C-(1-oxo-but-2-ene-1,4-diyl)-2,3-dideoxy-α-D-glucopyranoside 

Relevant articles and documents

Stereoselective synthesis of seven-membered lactams and lactones on a carbohydrate scaffold using ring-closing metathesis

We present here the application of Grubbs' 2nd generation catalyst for the ring-closing metathesis of electron-deficient α,β-unsaturated amides and esters leading to the synthesis of enantiopure azepinone and oxepinone derivatives on a carbohydrate glycos