Neryl glucoside

Base Information

Chemical Name:Neryl glucoside
CAS No.:22850-13-1
Molecular Formula:C16H28O6
Molecular Weight:316.395
Hs Code.:2938900000
Mol file:22850-13-1.mol

Synonyms:Neryl glucoside;2-[(2Z)-3,7-dimethylocta-2,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol;CHEBI:169359

Suppliers and Price of Neryl glucoside

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
Geranyl b-D-glucoside
2mg
$ 468.00

Biosynth Carbosynth
Geranyl b-D-glucoside
10 mg
$ 450.00

Biosynth Carbosynth
Geranyl b-D-glucoside
5 mg
$ 300.00

Biosynth Carbosynth
Geranyl b-D-glucoside
2 mg
$ 150.00

Biosynth Carbosynth
Geranyl b-D-glucoside
1 mg
$ 95.00

Biosynth Carbosynth
Geranyl b-D-glucoside
25 mg
$ 625.00

AK Scientific
Nerylglucoside
10mg
$ 657.00

AK Scientific
Nerylglucoside
1mg
$ 178.00

Total 4 raw suppliers

Chemical Property of Neryl glucoside

Chemical Property:

PSA：99.38000
LogP:0.49560
XLogP3:1.2
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:316.18858861
Heavy Atom Count:22
Complexity:388

Purity/Quality:

97% ^*data from raw suppliers

Geranyl b-D-glucoside ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCCC(=CCOC1C(C(C(C(O1)CO)O)O)O)C)C
Isomeric SMILES:CC(=CCC/C(=C\COC1C(C(C(C(O1)CO)O)O)O)/C)C

Technology Process of Neryl glucoside

There total 2 articles about Neryl glucoside 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:

: 84534-31-6
(E)-3,7-dimethylocta-2,6-dien-1-yl [α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranoside]

: 3615-41-6,478518-52-4
L-Rhamnose

: 22850-13-1
geranyl O-β-D-glucopyranoside

Guidance literature:: With α-L-rhamnopyranosidase; In water; at 40 ℃; for 1.5h; Product distribution; 0.1M acetate buffer (pH=4.2), mechanism of action of enzyme;
DOI:10.1016/0008-6215(88)80012-0

Reference yield:

: 84582-22-9,84534-32-7
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]oxane-3,4,5-triol

: 5328-37-0
L-arabinose

: 22850-13-1
geranyl O-β-D-glucopyranoside

Guidance literature:: With α-L-arabinofuranosidase; In water; at 40 ℃; for 16h; Product distribution; 0.1M acetate buffer (pH=4.2), mechanism of action of enzyme;
DOI:10.1016/0008-6215(88)80012-0

Reference yield:

: 22850-13-1
geranyl O-β-D-glucopyranoside

: 150995-11-2,152520-94-0,197508-58-0
geranyl 6-O-β-D-xylopyranosyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 63 percent / DMAP / pyridine / 24 h / 20 °C

2: 71 percent / pyridine / 12 h / 20 °C

3: 99 percent / HCl / tetrahydrofuran / 12 h / 20 °C

4: 93 percent / tetramethylurea; AgOTf / CH₂Cl₂ / 18 h / 20 °C

5: 71 percent / NaOMe / methanol; tetrahydrofuran / 0.5 h / 20 °C

With hydrogenchloride; dmap; sodium methylate; silver trifluoromethanesulfonate; tetramethylurea; In tetrahydrofuran; pyridine; methanol; dichloromethane;
DOI:10.3987/COM-05-10640