Lyxoflavine

Base Information Edit

Chemical Name:Lyxoflavine
CAS No.:13123-37-0
Molecular Formula:C₁₇H₂₀N₄O₆
Molecular Weight:376.369
Hs Code.:
UNII:STP460337X
DSSTox Substance ID:DTXSID001127504
Nikkaji Number:J5.784C
Wikidata:Q27289394
Mol file:13123-37-0.mol

Synonyms:Lyxoflavine;Lyxoflavine [MI];13123-37-0;NSC-18343;UNII-STP460337X;STP460337X;L-Arabinitol, 5-deoxy-5-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo(g)pteridin-10(2H)-yl)-;7,8-dimethyl-10-((2S,3S,4S)-2,3,4,5-tetrahydroxypentyl)benzo[g]pteridine-2,4(3H,10H)-dione;L-Arabinitol, 5-deoxy-5-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo[g]pteridin-10(2H)-yl)-;SCHEMBL5899262;DTXSID001127504;AKOS040752863;5-Deoxy-5-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo[g]pteridin-10(2H)-yl)-L-arabinitol;7,8-dimethyl-10-[(2S,3S,4S)-2,3,4,5-tetrahydroxypentyl]benzo[g]pteridine-2,4-dione;482-12-2;Q27289394;75598-82-2

Suppliers and Price of Lyxoflavine

Supply Marketing:Edit

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 Lyxoflavine Edit

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.65g/cm³
XLogP3:-1.5
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:376.13828437
Heavy Atom Count:27
Complexity:680

Purity/Quality:: 99%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(CO)O)O)O
Isomeric SMILES:CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@H](CO)O)O)O

Technology Process of Lyxoflavine

There total 11 articles about Lyxoflavine 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:

: 13345-95-4,78692-23-6
1,5-dihydro-riboflavin

: 1464-43-3,2897-21-4,26932-45-6,29621-88-3
seleno-L-cystine

: 3614-08-2,10236-58-5,18312-66-8,176300-66-6
L-selenocysteine

: 83-88-5,482-11-1,482-12-2,3687-62-5,5978-87-0,13123-37-0,33210-89-8,35919-91-6,53187-51-2,53187-52-3,135681-43-5,42880-33-1
riboflavin

Guidance literature:: In aq. phosphate buffer; at 25 ℃; for 6h; pH=7; pH-value; Equilibrium constant;
DOI:10.1002/kin.21430

Reference yield:

: 95-64-7
4-amino-o-xylene

: 83-88-5,482-11-1,482-12-2,3687-62-5,5978-87-0,13123-37-0,33210-89-8,35919-91-6,53187-51-2,53187-52-3,135681-43-5,42880-33-1
riboflavin

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium cyanoborohydride / methanol / 48 h / Reflux

2.1: hydrogenchloride / water / 0.17 h / 0 °C

2.2: 0.5 h / 0 °C

3.1: butan-1-ol; acetic acid / 5 h / Reflux

With hydrogenchloride; sodium cyanoborohydride; In methanol; water; acetic acid; butan-1-ol;
DOI:10.1021/acs.joc.6b00640

Reference yield:

: 50-69-1
D-ribose

: 83-88-5,482-11-1,482-12-2,3687-62-5,5978-87-0,13123-37-0,33210-89-8,35919-91-6,53187-51-2,53187-52-3,135681-43-5,42880-33-1
riboflavin

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium cyanoborohydride / methanol / 48 h / Reflux

2.1: hydrogenchloride / water / 0.17 h / 0 °C

2.2: 0.5 h / 0 °C

3.1: butan-1-ol; acetic acid / 5 h / Reflux

With hydrogenchloride; sodium cyanoborohydride; In methanol; water; acetic acid; butan-1-ol;
DOI:10.1021/acs.joc.6b00640