5'-noraristeromycin

Base Information

Chemical Name:5'-noraristeromycin
CAS No.:142635-42-5
Molecular Formula:C₁₀H₁₃N₅O₃
Molecular Weight:251.245
Hs Code.:
Mol file:142635-42-5.mol

Synonyms:1,2,3-Cyclopentanetriol,4-(6-amino-9H-purin-9-yl)-, (1a,2b,3b,4a)- (9CI); 1,2,3-Cyclopentanetriol, 4-(6-amino-9H-purin-9-yl)-, (1a,2b,3b,4a)-(?à)-; (?à)-5'-Noraristeromycin

Suppliers and Price of 5'-noraristeromycin

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 3 raw suppliers

Chemical Property of 5'-noraristeromycin

Chemical Property:

Boiling Point:563.7°Cat760mmHg
Flash Point:294.7°C
PSA：130.31000
Density:2.06g/cm³
LogP:-0.98280

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 5'-noraristeromycin

There total 6 articles about 5'-noraristeromycin 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: 65.0%

: 142635-46-9
(+/-)-(1α,2β,3β,4α)-4-(6-chloro-9H-purin-9-yl)-1,2,3-cyclopentanetriol

: 142635-42-5
(+/-)-5'-Noraristeromycin

Guidance literature:: With ammonia; In methanol; at 140 ℃; for 48h;
DOI:10.1021/jm00096a012

Reference yield:

: 7129-41-1,54460-11-6
6-oxabicyclo<3.1.0>hex-2-ene

: 142635-42-5
(+/-)-5'-Noraristeromycin

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / <(i-C₃H₇O)3P>4Pd / tetrahydrofuran; dimethylsulfoxide / 1.) 0 deg C for 3 h 2.) 25 deg C overnight

2: osmium tetroxide, N-methyl-morpholine N-oxide

With osmium(VIII) oxide; 4-methylmorpholine N-oxide; C₃₆H₈₄O₁₂P₄Pd; In tetrahydrofuran; dimethyl sulfoxide;
DOI:10.1021/ja00210a064

Reference yield:

: 66224-66-6,66224-67-7,66224-68-8,66224-69-9,134434-48-3,134434-49-4,134454-76-5,134461-75-9
adenine

: 142635-42-5
(+/-)-5'-Noraristeromycin

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / <(i-C₃H₇O)3P>4Pd / tetrahydrofuran; dimethylsulfoxide / 1.) 0 deg C for 3 h 2.) 25 deg C overnight

2: osmium tetroxide, N-methyl-morpholine N-oxide

With osmium(VIII) oxide; 4-methylmorpholine N-oxide; C₃₆H₈₄O₁₂P₄Pd; In tetrahydrofuran; dimethyl sulfoxide;
DOI:10.1021/ja00210a064