(1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol

Base Information

Chemical Name:(1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol
CAS No.:5338-40-9
Molecular Formula:C12H16N2O5
Molecular Weight:268.2658
Hs Code.:
DSSTox Substance ID:DTXSID701267084
Mol file:5338-40-9.mol

Synonyms:5338-40-9;DTXSID701267084;(1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol

Suppliers and Price of (1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol

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 (1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol

Chemical Property:

Vapor Pressure:6.5E-23mmHg at 25°C
Refractive Index:1.744
Boiling Point:738.7°Cat760mmHg
Flash Point:400.6°C
Density:1.607g/cm³
XLogP3:-1.9
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:268.10592162
Heavy Atom Count:19
Complexity:293

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)C(C(C(C(CO)O)O)O)O
Isomeric SMILES:C1=CC=C2C(=C1)NC(=N2)[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O

Technology Process of (1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol

There total 7 articles about (1R)-1-C-1H-Benzimidazol-2-yl-D-arabinitol 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:

: 3458-28-4
D-Mannose

: 95-54-5
1,2-diamino-benzene

: 5338-40-9
(1'R,2'R,3'R,4'R)-2-[1',2',3',4',5'-pentahydroxypentyl]-1H-benzimidazole

Guidance literature:: With iodine; acetic acid; In methanol; at 20 ℃; for 12h;
DOI:10.1021/jo800234x

Reference yield:

: 642-99-9
mannonic acid

: 95-54-5
1,2-diamino-benzene

: 5338-40-9
(1'R,2'R,3'R,4'R)-2-[1',2',3',4',5'-pentahydroxypentyl]-1H-benzimidazole

Guidance literature:: With hydrogenchloride; phosphoric acid;

Reference yield:

: 3458-28-4
D-Mannose

: 5338-40-9
(1'R,2'R,3'R,4'R)-2-[1',2',3',4',5'-pentahydroxypentyl]-1H-benzimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: concentrated sulfuric acid

2: aqueous KOH-solution; potassium permanganate

3: aqueous HCl

With hydrogenchloride; potassium hydroxide; potassium permanganate; sulfuric acid;