Orthonitrophenyl-beta-D-fucopyranoside

Base Information

• Chemical Name: Orthonitrophenyl-beta-D-fucopyranoside
• CAS No.: 1154-94-5
• Molecular Formula: C₁₂H₁₅NO₇
• Molecular Weight: 285.254
• Hs Code.: 29389090
• DSSTox Substance ID: DTXSID80921729
• Nikkaji Number: J489.550I
• Wikidata: Q2928817
• Metabolomics Workbench ID: 52379
• Mol file: 1154-94-5.mol

Synonyms:2-nitrophenyl-beta-fucoside;ONPF

Chemical Property of Orthonitrophenyl-beta-D-fucopyranoside

Chemical Property:

• Vapor Pressure: 4.53E-11mmHg at 25°C
• Boiling Point: 506.2°Cat760mmHg
• Flash Point: 260°C
• PSA: 124.97000
• Density: 1.503g/cm³
• LogP: 0.32430
• Storage Temp.: −20°C
• XLogP3: -0.7
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 285.08485182
• Heavy Atom Count: 20
• Complexity: 347

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-Nitrophenyl b-D-fucopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1C(C(C(C(O1)OC2=CC=CC=C2[N+](=O)[O-])O)O)O
• Isomeric SMILES: C[C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)OC2=CC=CC=C2[N+](=O)[O-])O)O)O
• Uses: substrate for b-D-mannosidases 2-Nitrophenyl β-D-Fucopyranoside (cas# 1154-94-5) is a compound useful in organic synthesis.

Technology Process of Orthonitrophenyl-beta-D-fucopyranoside

There total 1 articles about Orthonitrophenyl-beta-D-fucopyranoside 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:

→ nitrophenyl-α-L-rhamnopyranoside (18918-28-0,1154-94-5)

Guidance literature:

Aus entspr. substit. Phenyl-2,3,4-triacetyl-α-L-rhamnosid, Na-Methanolat in abs. Me. (Siedetemp.);