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经验公式(希尔记法):
C28H40O10
化学文摘社编号:
分子量:
536.61
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1632489
Assay:
98%
Form:
solid
InChI
1S/C28H40O10/c1-2-6-26-25(5-1)35-21-17-31-13-9-29-11-15-33-19-23-37-27-7-3-4-8-28(27)38-24-20-34-16-12-30-10-14-32-18-22-36-26/h1-8H,9-24H2
SMILES string
C1COCCOc2ccccc2OCCOCCOCCOCCOc3ccccc3OCCOCCO1
InChI key
MXCSCGGRLMRZMF-UHFFFAOYSA-N
assay
98%
form
solid
Quality Level
reaction suitability
core: crown ether
mp
106-108 °C (lit.)
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Oana Buriac et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-23)
Platinum is a precious metal with many applications, such as: catalytic converters, laboratory equipment, electrical contacts and electrodes, digital thermometers, dentistry, and jewellery. Due to its broad usage, it is essential to recover it from waste solutions resulted out of
Jia-Bin Guo et al.
Organic letters, 13(20), 5688-5691 (2011-10-04)
A triptycene-derived macrotricyclic host containing two dibenzo-[30]-crown-10 moieties forms stable 1:2 host-guest complexes with paraquat derivatives in both solution and the solid state, in which anion-π interactions between PF(6)(-) and the bipyridinium rings play an important role. Moreover, it was
Ahmed Khudhair Hassan et al.
Sensors (Basel, Switzerland), 11(1), 1028-1042 (2012-02-22)
Plasticised poly(vinyl chloride)-based membranes containing the ionophores (α-, β- and γ-cyclodextrins (CD), dibenzo-18-crown-6 (DB18C6) and dibenzo-30-crown-10 (DB30C10) were evaluated for their potentiometric response towards promethazine (PM) in a flow injection analysis (FIA) set-up. Good responses were obtained when β- and
Marko Marjanović et al.
Journal of medicinal chemistry, 50(5), 1007-1018 (2007-02-16)
The present paper demonstrates the antiproliferative ability and structure-activity relationships (SAR) of 14 crown and aza-crown ether analogues on five tumor-cell types. The most active compounds were di-tert-butyldicyclohexano-18-crown-6 (3), which exhibited cytotoxicity in the submicromolar range, and di-tert-butyldibenzo-18-crown-6 (5) (IC50
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