82598-84-3

Basic information

• Product Name: 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactonic Acid d-Lactone
• Synonyms: 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactonic Acid d-Lactone;2,3,4,6-Tetra-O-benzyl-D-galactono-1,5-lactone;2,3,4,6-Tetrakis-O-(phenylMethyl)-D-galactonic Acid δ-Lactone
• CAS NO: 82598-84-3
• Molecular Formula: C₃₄H₃₄O₆
• Molecular Weight: 0
• Product Categories: Carbohydrates & Derivatives
• Mol File: 82598-84-3.mol
• Article Data: 26

Chemical Properties

• Appearance: /
• Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
• Solubility: Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly)
• Stability: Hygroscopic
• CAS DataBase Reference: 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactonic Acid d-Lactone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactonic Acid d-Lactone(82598-84-3)
• EPA Substance Registry System: 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactonic Acid d-Lactone(82598-84-3)

Safety Data

• Hazardous Substances Data: 82598-84-3(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 82598-84-3 differently. You can refer to the following data:
1. 2,3,4,6-Tetrakis-O-(phenylmethyl)-D-galactonic Acid d-Lactone is used in peptide coupling reactions.
2. It is used in peptide coupling reactions.

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 167904-03-2 2,3,4,6-tetra-O-benzyl-D-galactononitrile 
• 10257-28-0 D-Galactose 
• 97-30-3 methyl D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 195827-82-8 methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside 
• 2595-07-5 allyl D-galactopyranoside 
• 214490-83-2 α,β-allyloxy-2,3,4,6-tetra-O-benzyl-d-galactose 
• 3396-99-4 methyl α-D-galactopyranoside 
• 53008-63-2 methyl 2,3,4,6-tetra-O-benzyl-α-D-galactopyranoside 
• 13992-16-0 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-galactopyranoside 
• 25878-60-8 D-galactose pentaacetate 
• 785806-29-3 thiophenyl 2,3,4,6-O-tetra-benzyl-α/β-D-galactopyranoside 
• 132748-02-8 O-(2,3,4,6-tetra-O-benzyl-α,β-D-galactopyranosyl)trichloroacetimidate 

Downstream Products

• 82659-57-2 3-(2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl)prop-1-ene 
• 82659-55-0 3-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)prop-1-ene 
• 160584-12-3 1-O-Acetyl-2,3,4,6-tetra-O-benzyl-1-(2-thiazolyl)-β-D-galactopyranose 
• 160584-11-2 1-O-Acetyl-2,3,4,6-tetra-O-benzyl-1-(2-thiazolyl)-α-D-galactopyranose 
• 160701-76-8 2,3,4,6-Tetra-O-benzyl-1-(2-thiazolyl)-α-D-galactopyranose 
• 145150-03-4 1,3,4,5,7-penta-O-benzyl-α-D-galacto-heptulopyranose 
• 179090-11-0 (3R,4S,5S,6R)-3,4,5-tris(benzyloxy)-6-[(benzyloxy)methyl]tetrahydro-2H-pyran-2-one 
• 414858-57-4 (2R,3R,4S,5S,6R)-3,4,5-tri(benzyloxy)-6-[(benzyloxy)methyl]-5,6-dihydro-2-[3-[(4-methoxybenzyloxy)methyl]-1,4-dithiin-2-yl]tetrahydro-2H-2-pyranol 
• 440677-32-7 2,3,4,6-tetra-O-benzyl-1-C-(2-benzothiazolyl)-α-D-galactopyranose 
• 477319-53-2 ((2R,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-ylmethyl)-phosphonic acid diethyl ester 
• 400888-39-3 ((2S,3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester 
• 219826-01-4 3,7-anhydro-4,5,6,8-tetra-O-acetyl-1,1,2,2-tetradehydro-1,2-D-glycero-L-mannooctitol 
• 219864-00-3 3,7-anhydro-4,5,6,8-tetra-O-benzyl-1,1,2,2-tetradehydro-1,2-D-glycero-L-mannooctitol 
• 219826-17-2 N-acetyl 3-C-(3,7-anhydro-4,5,6,8-tetra-O-acetyl-1,1,2,2-tetradehydro-1,2-D-glycero-D-mannooctityl)-DL-phenylalanine methyl ester 

Relevant articles and documents

Stereoselective Palladium-Catalyzed Arylation of Exo-Glycals with Aryl Iodides

A novel methodology for the arylation of exo-glycals has been developed. A range of exo-glycals underwent reactions with aryl iodides in the presence of a palladium catalyst. The transformation proceeded in a stereoselective manner to afford Z-isomers. Th

Highly (Z)-Diastereoselective Synthesis of Trifluoromethylated exo-Glycals via Photoredox and Copper Catalysis

Highly (Z)-diastereoselective approaches for the synthesis of trifluoromethylated exo-glycals by copper and photoredox catalysis are described. These complementary reactions are applicable to a wide range of methylene exo-glycals generated from the corresponding pyranoses and furanoses and give trifluoromethylated compounds under mild conditions in moderate to good yields. DFT calculations have allowed a rationalization of the observed (Z)-stereoselectivity.

Iodine monochloride (ICl) as a highly efficient, green oxidant for the oxidation of alcohols to corresponding carbonyl compounds

Iodine monochloride (ICl) was discovered to be a highly efficient, green oxidant, which can oxidize aldose hemiacetals, diarylmethanols, arylalkylmethanols, anddialkylmethanols to the corresponding aldose lactones, diarylmethanones, arylalkylmethanones, and dialkylmethanones, respectively, in high yields. ICl as a green, metal-free oxidant is characterized by mild reaction condition, short reaction time, good yield, and broad scope.