Drfbpi

Base Information

Chemical Name:Drfbpi
CAS No.:143632-16-0
Molecular Formula:C21H21 N3 O4
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID30931974
Nikkaji Number:J2.098.077J
Mol file:143632-16-0.mol

Synonyms:1-(2-deoxy-beta-D-ribofuranosyl)-4-(3-benzamido)phenylimidazole;1-(2-deoxyribofuranosyl)-4-(3-benzamido)phenylimidazole;dRFBPI

Suppliers and Price of Drfbpi

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Drfbpi

Chemical Property:

Vapor Pressure:1.9E-16mmHg at 25°C
Boiling Point:624.3°Cat760mmHg
Flash Point:331.4°C
PSA：100.10000
Density:1.37g/cm³
LogP:2.82710
XLogP3:1.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:379.15320616
Heavy Atom Count:28
Complexity:528

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(OC1N2C=C(N=C2)C3=CC(=CC=C3)NC(=O)C4=CC=CC=C4)CO)O
Isomeric SMILES:C1[C@@H]([C@H](O[C@H]1N2C=C(N=C2)C3=CC(=CC=C3)NC(=O)C4=CC=CC=C4)CO)O

Technology Process of Drfbpi

There total 8 articles about Drfbpi 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:

: 4330-21-6
2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride

: 143632-16-0
1-(2-deoxy-β-D-ribofuranosyl)-4-(3-benzamidophenyl)imidazole

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH / 1.) CH₃CN, 0 deg C, 40 min, 2.) CH₃CN, 3 h

2: 99 percent / 1percent methanol. NaOH / 1 h / Ambient temperature

3: 99 percent / H₂ / 5percent Pd/C / methanol / 2 h / Ambient temperature

4: pyridine / 0.5 h / 0 °C

5: pyridine / 2.5 h / Ambient temperature

6: sat. aq. NH₄OH / 1 h / 0 - 20 °C

With pyridine; ammonium hydroxide; sodium hydroxide; hydrogen; sodium hydride; palladium on activated charcoal; In methanol;

Reference yield:

: 143632-14-8
1-(2-deoxy-β-D-ribofuranosyl)-4-(3-nitrophenyl)imidazole

: 143632-16-0
1-(2-deoxy-β-D-ribofuranosyl)-4-(3-benzamidophenyl)imidazole

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / H₂ / 5percent Pd/C / methanol / 2 h / Ambient temperature

2: pyridine / 0.5 h / 0 °C

3: pyridine / 2.5 h / Ambient temperature

4: sat. aq. NH₄OH / 1 h / 0 - 20 °C

With pyridine; ammonium hydroxide; hydrogen; palladium on activated charcoal; In methanol;

Reference yield:

: 143632-13-7
1-<2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-ribofuranosyl>-4-(3-nitrophenyl)imidazole

: 143632-16-0
1-(2-deoxy-β-D-ribofuranosyl)-4-(3-benzamidophenyl)imidazole

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / 1percent methanol. NaOH / 1 h / Ambient temperature

2: 99 percent / H₂ / 5percent Pd/C / methanol / 2 h / Ambient temperature

3: pyridine / 0.5 h / 0 °C

4: pyridine / 2.5 h / Ambient temperature

5: sat. aq. NH₄OH / 1 h / 0 - 20 °C

With pyridine; ammonium hydroxide; sodium hydroxide; hydrogen; palladium on activated charcoal; In methanol;