Araboflavin, D-

Base Information

Chemical Name:Araboflavin, D-
CAS No.:5978-87-0
Molecular Formula:C₁₇H₂₀N₄O₆
Molecular Weight:376.369
Hs Code.:
UNII:U16E01V13F
Nikkaji Number:J15.732E
Wikidata:Q27290548
Mol file:5978-87-0.mol

Synonyms:D-Arabinoflavine;Araboflavin, D-;D-Araboflavin [MI];D-Araboflavin;UNII-U16E01V13F;U16E01V13F;5978-87-0;D-Arabinitol, 1-deoxy-1-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo(g)pteridin-10(2H)-yl)-;1-Deoxy-1-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo(g)pteridin-10(2H)-yl)-D-arabinitol;1-Deoxy-1-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo[g]pteridin-10(2H)-yl)-D-arabinitol;D-Arabinitol, 1-deoxy-1-(3,4-dihydro-7,8-dimethyl-2,4-dioxobenzo[g]pteridin-10(2H)-yl)-;6,7-dimethyl-9-D-araboflavin;SCHEMBL12979917;Q27290548;Isoalloxazine, 7,8-dimethyl-10-(D-arabino-2,3,4,5-tetrahydroxypentyl)-;7,8-dimethyl-10-(arabino-2,3,4,5-tetrahydroxypentyl)benzo[g]pteridine-2,4(3H,10H)-dione

Suppliers and Price of Araboflavin, D-

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

American Custom Chemicals Corporation
D-ARABOFLAVIN 95.00%
5MG
$ 496.24

Total 1 raw suppliers

Chemical Property of Araboflavin, D-

Chemical Property:

Melting Point:302-303°
PSA：161.56000
Density:1.65g/cm³
LogP:-1.67520
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:

98% ^*data from raw suppliers

D-ARABOFLAVIN 95.00% ^*data from reagent 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 Araboflavin, D-

There total 10 articles about Araboflavin, D- 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