(-)-trans-Carveol glucoside

Base Information

Chemical Name:(-)-trans-Carveol glucoside
CAS No.:113349-30-7
Molecular Formula:C₁₆H₂₆O₆
Molecular Weight:314.379
Hs Code.:
DSSTox Substance ID:DTXSID501145236
Nikkaji Number:J700.229G
Wikidata:Q76415919
Metabolomics Workbench ID:44086

Synonyms:(-)-trans-Carveol glucoside;CHEBI:172544;DTXSID501145236;5beta-Isopropenyl-2-methyl-2-cyclohexene-1alpha-yl beta-D-glucopyranoside;(1S,5R)-2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-yl beta-D-glucopyranoside;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(1S,5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-yl]oxyoxane-3,4,5-triol;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-{[(1S,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl]oxy}oxane-3,4,5-triol;113349-30-7

Suppliers and Price of (-)-trans-Carveol glucoside

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (-)-trans-Carveol glucoside

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:314.17293854
Heavy Atom Count:22
Complexity:434

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(=C)C
Isomeric SMILES:CC1=CC[C@H](C[C@@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C(=C)C

Technology Process of (-)-trans-Carveol glucoside

There total 8 articles about (-)-trans-Carveol 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: 89.0%

: 2,2-Dimethyl-propionic acid (2R,3R,4R,5R,6R)-3-(2,2-dimethyl-propionyloxy)-2-(2,2-dimethyl-propionyloxymethyl)-5-hydroxy-6-((1S,5R)-5-isopropenyl-2-methyl-cyclohex-2-enyloxy)-tetrahydro-pyran-4-yl ester

: 113349-30-7
(2R,3S,4S,5R,6R)-2-Hydroxymethyl-6-((1S,5R)-5-isopropenyl-2-methyl-cyclohex-2-enyloxy)-tetrahydro-pyran-3,4,5-triol

Guidance literature:: With Amberlite IRA₄₀₀ (OH^-); In methanol; for 16h; Heating;
DOI:10.1016/S0040-4039(97)10315-X

Reference yield:

: 117861-56-0,117895-56-4,129831-53-4
Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(5-isopropenyl-2-methyl-cyclohex-2-enyloxy)-tetrahydro-pyran-3-yl ester

: 74284-29-0,113349-30-7,114673-98-2
(2R,3S,4S,5R,6R)-2-Hydroxymethyl-6-(5-isopropenyl-2-methyl-cyclohex-2-enyloxy)-tetrahydro-pyran-3,4,5-triol

Guidance literature:: With Amberlyst A-26; In methanol; at 20 ℃; for 3h; Yield given;

Reference yield:

: 149198-97-0,104445-19-4
3,4,6-tri-O-pivaloyl-D-glucal

: 113349-30-7
(2R,3S,4S,5R,6R)-2-Hydroxymethyl-6-((1S,5R)-5-isopropenyl-2-methyl-cyclohex-2-enyloxy)-tetrahydro-pyran-3,4,5-triol

Guidance literature:: Multi-step reaction with 3 steps

1: 66 percent / 2,2-dimethyldioxirane / acetone

2: 33 percent / SiO₂, molecular sieves 3 Angstroem / benzene / 24 h / Ambient temperature

3: 89 percent / Amberlite IRA₄₀₀ (OH^-) / methanol / 16 h / Heating

With 2,2-dimethyldioxirane; 3 A molecular sieve; Amberlite IRA₄₀₀ (OH^-); silica gel; In methanol; acetone; benzene;
DOI:10.1016/S0040-4039(97)10315-X