6-Bromo-2-naphthyl beta-D-xylopyranoside

Base Information

• Chemical Name: 6-Bromo-2-naphthyl beta-D-xylopyranoside
• CAS No.: 69594-75-8
• Molecular Formula: C15H15BrO5
• Molecular Weight: 355.185
• Hs Code.: 2932999099
• European Community (EC) Number: 274-053-5
• DSSTox Substance ID: DTXSID50219862
• Nikkaji Number: J318.009C
• Wikidata: Q72448308
• Mol file: 69594-75-8.mol

Synonyms:69594-75-8;6-Bromo-2-naphthyl b-D-xylopyranoside;6-Bromo-2-naphthyl beta-D-xylopyranoside;2-(6-BROMONAPHTHYL)-BETA-D-XYLOPYRANOSIDE;(2S,3R,4S,5R)-2-(6-bromonaphthalen-2-yl)oxyoxane-3,4,5-triol;EINECS 274-053-5;B-D-XYLOPYRANOSIDE,6-BROMO-2-NAPHTHALENYL (9CI);C15H15BrO5;SCHEMBL4609050;C15-H15-Br-O5;DTXSID50219862;MFCD00076065;CS-0206285;6-Bromo-2-naphthalenyl beta-D-xylopyranoside;b-D-Xylopyranoside,6-bromo-2-naphthalenyl(9ci);(2S,3R,4S,5R)-2-((6-Bromonaphthalen-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triol;(2S,3R,4S,5R)-2-(6-bromonaphthalen-2-yloxy)tetrahydro-2H-pyran-3,4,5-triol

Chemical Property of 6-Bromo-2-naphthyl beta-D-xylopyranoside

Chemical Property:

• Melting Point: 190 °C
• Boiling Point: 553.9 °C at 760 mmHg
• Flash Point: 288.8 °C
• PSA: 79.15000
• Density: 1.705 g/cm³
• LogP: 1.42010
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 354.01029
• Heavy Atom Count: 21
• Complexity: 355

Purity/Quality:

98% ^*data from raw suppliers

6-Bromo-2-naphthylbeta-D-xylopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C(C(C(O1)OC2=CC3=C(C=C2)C=C(C=C3)Br)O)O)O
• Isomeric SMILES: C1[C@H]([C@@H]([C@H]([C@@H](O1)OC2=CC3=C(C=C2)C=C(C=C3)Br)O)O)O

Technology Process of 6-Bromo-2-naphthyl beta-D-xylopyranoside

There total 3 articles about 6-Bromo-2-naphthyl beta-D-xylopyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

(6-bromo-[2]naphthyl)-(tri-O-acetyl-β-D-ribopyranoside) → (6-bromo-[2]naphthyl)-β-D-ribopyranoside (69594-75-8)

Guidance literature:

With ammonia;

DOI:10.1021/ja01132a034

Reference yield:

6-bromo-naphthalen-2-ol (15231-91-1) → (6-bromo-[2]naphthyl)-β-D-ribopyranoside (69594-75-8)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / Erwaermen unter vermindertem Druck

2: methanol. ammonia

With ammonia; toluene-4-sulfonic acid;

DOI:10.1021/ja01132a034

Reference yield:

1,2,3,4-tetra-O-acetyl-β-D-ribopyranose (4627-30-9) → (6-bromo-[2]naphthyl)-β-D-ribopyranoside (69594-75-8)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / Erwaermen unter vermindertem Druck

2: methanol. ammonia

With ammonia; toluene-4-sulfonic acid;

DOI:10.1021/ja01132a034

upstream raw materials:

6-bromo-naphthalen-2-ol

1,2,3,4-tetra-O-acetyl-β-D-ribopyranose