Catalogue Number
AV-S05717
Analysis Method
HPLC,NMR,MS
Specification
98%
Storage
2-8°C
Molecular Weight
536.53
Appearance
Powder
Botanical Source
Schisandra chinensis
Structure Type
Lignans
Category
Standards;Natural Pytochemical;API
SMILES
COC1=C(C=CC(=C1)C2C3COC(C3(CO2)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O
Synonyms
(1S,3aS,4R,6aR)-1,4-Bis(4-hydroxy-3-methoxyphenyl)dihydro-1H,3H-furo[3,4-c]furan-3a(4H)-yl β-D-glucopyranoside/β-D-Glucopyranoside, (1S,3aS,4R,6aR)-dihydro-1,4-bis(4-hydroxy-3-methoxyphenyl)-1H,3H-furo[3,4-c]furan-3a(4H)-yl
IUPAC Name
(2S,3R,4S,5S,6R)-2-[[(3R,3aS,6S,6aR)-3,6-bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Density
1.6±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
425.9±32.9 °C
Boiling Point
780.7±60.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C26H32O12/c1-33-17-7-12(3-5-15(17)28)23-14-10-35-24(13-4-6-16(29)18(8-13)34-2)26(14,11-36-23)38-25-22(32)21(31)20(30)19(9-27)37-25/h3-8,14,19-25,27-32H,9-11H2,1-2H3/t14-,19-,20-,21+,22-,23-,24-,25+,26-/m1/s1
InChl Key
DRAPQDCEBKBPQE-ACFZRETJSA-N
WGK Germany
RID/ADR
HS Code Reference
2933990000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:81495-71-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
23148512
Two new compounds (triterpenoid saponin and heterocyclic compound), 2α,3β, 19α,23,30-pentahydroxyurs-12-en-28-oic acid-28-O-β-d-glucopyranosyl ester (1) and N-hydroxyl-hexahydroazepin-2,4-diones (2), with 11 known compounds, picein (3), (7S,8R)-dihydrodehydrodiconiferyl alcohol-9′-O-β-d-glucopyranoside (4), (+)-1-hydroxy-2-epipinoresinol-1-β-d-glucoside (5), (+)-1-hydroxypinoresinol-1-β-d-glucoside (6), (+)-1-hydroxypinoresinol-4′-β-d-glucoside (7), schaftside (6-C-β-d-glucopyranosyl-8-C-α-l-arabinosyl apigenin) (8), isoschaftside (6-C-α-l-arabinosyl-8-C-β-d-glucopyranosyl apigenin) (9), isorhamnetin-3-O-β-d-glucopyranoside (10), quercetin-3-O-β-glucuronide (11), 8-O-methylherbacetin-3-O-sophoroside (12) and kaempferol (13), were isolated from Potentilla multicaulis Bunge. The structure of the compounds was elucidated by chemical and spectral evidence.
Two new compounds from Potentilla multicaulis Bunge.
Jia L1, Wang J, Lv C, Xu T, He L, Dong Y, Lu J.
2013 Aug
