1-Amino-1-deoxy-D-ribitol

Base Information

Chemical Name:1-Amino-1-deoxy-D-ribitol
CAS No.:527-47-9
Molecular Formula:C₅H₁₃NO₄
Molecular Weight:151.163
Hs Code.:
Mol file:527-47-9.mol

Synonyms:1-Amino-1-deoxy-D-ribitol;D-Ribamine;D-Ribitylamine

Suppliers and Price of 1-Amino-1-deoxy-D-ribitol

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

Usbiological
1-Amino-1-deoxy-D-ribitol
25mg
$ 715.00

TRC
1-Amino-1-deoxy-D-ribitol
100mg
$ 1155.00

Total 7 raw suppliers

Chemical Property of 1-Amino-1-deoxy-D-ribitol

Chemical Property:

PSA：106.94000
LogP:-2.27960

Purity/Quality:

98%min ^*data from raw suppliers

1-Amino-1-deoxy-D-ribitol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 1-Amino-1-deoxy-D-ribitol is an intermediate in synthesizing 5-Nitroso-6-ribitylamino-2,4(1H,3H)-pyrimidinedione (N546605), an inhibitor of lumazine synthase from spinach and the fungus Magnaporthe grisea.

Technology Process of 1-Amino-1-deoxy-D-ribitol

There total 1 articles about 1-Amino-1-deoxy-D-ribitol 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:

: 7647-01-0,15364-23-5
hydrogenchloride

: 1-(3-oxo-1-methyl-butylidenamino)-1-deoxy-D-ribitol

: 527-47-9,5657-44-3,42015-12-3,51108-70-4,54676-23-2,55700-82-8,55700-83-9,60537-18-0,69686-08-4,132881-75-5
D-Ribamin

: 123-54-6,81235-32-7
acetylacetone

Guidance literature:: at 20 ℃;

Reference yield: 86.0%

: 527-47-9,5657-44-3,42015-12-3,51108-70-4,54676-23-2,55700-82-8,55700-83-9,60537-18-0,69686-08-4,132881-75-5
D-Ribamin

: 1272385-09-7
4-(dibromomethyl)-5-chlorocarbonyl-2-(4-chlorophenyl)thiazole

: 4-(dibromomethyl)-2-(4-chlorophenyl)-N-(ribityl)thiazole-5-carboxamide

Guidance literature:: at 23 ℃; Inert atmosphere;
DOI:10.1021/jm1013538

Reference yield:

: 527-47-9,5657-44-3,42015-12-3,51108-70-4,54676-23-2,55700-82-8,55700-83-9,60537-18-0,69686-08-4,132881-75-5
D-Ribamin

: C₁₃H₂₀N₄O₆

: C₁₃H₂₀N₄O₆

: 2535-20-8,5118-16-1
6,7-dimethyl-8-ribityllumazine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / water; ethanol / 24 h / 20 °C / pH 8

2: acetic acid; iron / water / 2 h / 90 °C

3: 3 h / 20 - 80 °C

With iron; acetic acid; sodium hydroxide; In ethanol; water;
DOI:10.1039/c9ob01436e