35784-51-1

Basic information

• Product Name: ethyl 2,3,4-tri-O-benzoyl-1-thio-β-D-glucopyranoside
• Synonyms: ethyl 2,3,4-tri-O-benzoyl-1-thio-β-D-glucopyranoside
• CAS NO: 35784-51-1
• Molecular Weight: 536.603
• Mol File: 35784-51-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2,3,4-tri-O-benzoyl-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2,3,4-tri-O-benzoyl-1-thio-β-D-glucopyranoside(35784-51-1)
• EPA Substance Registry System: ethyl 2,3,4-tri-O-benzoyl-1-thio-β-D-glucopyranoside(35784-51-1)

Safety Data

• Hazardous Substances Data: 35784-51-1(Hazardous Substances Data)

Downstream Products

• 136005-84-0 Ethyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-1-thio-β-D-glucopyranoside 
• 136005-85-1 C₄₁H₄₄O₁₅S 
• 136005-85-1 C₄₁H₄₄O₁₅S 
• 136005-87-3 Ethyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside 
• 136005-86-2 C₄₃H₄₆O₁₇S 
• 136005-86-2 C₄₃H₄₆O₁₇S 
• 143995-75-9 ethyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-1-thio-β-D-glucopyranoside 
• 127840-77-1 ethyl 2,3,4-tri-O-benzoyl-6-O-(2',3',4',6'-tetra-O-benzyl-α-D-glucopyranosyl)-1-thio-β-D-glucopyranoside 
• 87562-76-3 kelampayoside A 
• 209113-73-5 3,4,5-trimethoxyphenyl 2,3,4-tri-O-phenoxyacetyl-6-O-(2,3-di-O-phenoxyacetyl-5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside 
• 209113-72-4 3,4,5-trimethoxyphenyl 6-O-(5-O-benzyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside 
• 209113-69-9 6-O-(2,3-di-O-acetyl-5-O-benzyl-β-D-erythro-apiofuranosyl)-2,3,4-tri-O-benzoyl-α-D-glucopyranosyl trichloroacetimidate 
• 209113-70-2 3,4,5-trimethoxyphenyl 6-O-(2,3-di-O-acetyl-5-O-benzyl-β-D-erythro-apiofuranosyl)-2,3,4-tri-O-benzoyl-β-D-glucopyranoside 
• 209113-74-6 3,4,5-trimethoxyphenyl 2,3,4-tri-O-phenoxyacetyl-6-O-(2,3-di-O-phenoxyacetyl-β-D-erythro-apiofuranosyl)-β-D-glucopyranoside 

Relevant articles and documents

Picoloyl protecting group in synthesis: Focus on a highly chemoselective catalytic removal

The picoloyl ester (Pico) has proven to be a versatile protecting group in carbohydrate chemistry. It can be used for the purpose of stereocontrolling glycosylations via an H-bond-mediated Aglycone Delivery (HAD) method. It can also be used as a temporary protecting group that can be efficiently introduced and chemoselectively cleaved in the presence of practically all other common protecting groups used in synthesis. Herein, we will describe a new method for rapid, catalytic, and highly chemoselective removal of the picoloyl group using inexpensive copper(ii) or iron(iii) salts. This journal is