226521
2-(Hydroxymethyl)anthraquinone
97%
Synonym(s):
2-Hydroxymethyl-9,10-anthracenedione
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About This Item
Empirical Formula (Hill Notation):
C15H10O3
CAS Number:
Molecular Weight:
238.24
Beilstein:
2120452
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
192-197 °C (lit.)
solubility
chloroform/methanol: 2%, clear to slightly hazy, colorless to yellow
functional group
hydroxyl
ketone
SMILES string
OCc1ccc2C(=O)c3ccccc3C(=O)c2c1
InChI
1S/C15H10O3/c16-8-9-5-6-12-13(7-9)15(18)11-4-2-1-3-10(11)14(12)17/h1-7,16H,8H2
InChI key
JYKHAJGLEVKEAA-UHFFFAOYSA-N
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Application
2-(Hydroxymethyl)anthraquinone (a photoremovable protecting group) was used to chemically cage (Z)-11-hexadecen-1-ol (sex pheromone of Chilo infuscatellus snellen).
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Five hexapeptide and heptapeptide analogs of luteinizing hormone-releasing hormone (LH-RH) were synthesized for use as carriers for cytotoxic compounds. These short analogs were expected to enhance target selectivity of the antineoplastic agents linked to them. Native LH-RH-(3-9) and LH-RH-(4-9) containing
Sanghamitra Atta et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 12(2), 393-403 (2012-10-31)
Photoremovable protecting groups (PRPGs) were demonstrated as a delivery device for controlled release of pheromone under both UV light (≥350 nm) and direct sunlight irradiation. In the present work, (Z)-11-hexadecen-1-ol (sex pheromone of Chilo infuscatellus Snellen) was chemically caged by
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To isolate and elucidate the constituents from stem of Chirita longgangensis var. hongyao. The constituents were extracted with methanol and isolated by chromatography on silica gel, Sephadex LH-20 and ODS. The structures were determined by NMR and MS spectral analysis.
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