5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose

Base Information

Chemical Name:5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose
CAS No.:4613-60-9
Molecular Formula:C15H19NO5
Molecular Weight:293.3151
Hs Code.:
NSC Number:170139
DSSTox Substance ID:DTXSID50305299

Synonyms:4613-60-9;NSC170139;DTXSID50305299;NSC-170139;5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose

Suppliers and Price of 5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose

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 2 raw suppliers

Chemical Property of 5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose

Chemical Property:

Vapor Pressure:7.34E-12mmHg at 25°C
Boiling Point:525.2°Cat760mmHg
Flash Point:271.5°C
Density:1.236g/cm³
XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:293.12632271
Heavy Atom Count:21
Complexity:394

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(OC2C(C(OC2O1)CNC(=O)C3=CC=CC=C3)O)C

Technology Process of 5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose

There total 3 articles about 5-Benzamido-5-deoxy-1,2-O-(1-methylethylidene)pentofuranose 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:

: 98-88-4
benzoyl chloride

: 4613-60-9
5-Benzamino-5-deoxy-1,2-isopropyliden-D-xylose

Guidance literature:: Multi-step reaction with 2 steps

1: lithium triethylborohydride / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

2: tetrahydrofuran / 48 h / 50 °C / Inert atmosphere

With lithium triethylborohydride; In tetrahydrofuran;
DOI:10.1021/acs.joc.6b00832