226521
2-（羟甲基）蒽醌
97%
别名:
2-羟甲基-9,10-蒽二酮
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关于此项目
经验公式（希尔记法）:
C15H10O3
化学文摘社编号:
分子量:
238.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-274-3
Beilstein/REAXYS Number:
2120452
MDL number:
产品名称
2-（羟甲基）蒽醌, 97%
InChI key
JYKHAJGLEVKEAA-UHFFFAOYSA-N
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
SMILES string
OCc1ccc2C(=O)c3ccccc3C(=O)c2c1
assay
97%
mp
192-197 °C (lit.)
solubility
chloroform/methanol: 2%, clear to slightly hazy, colorless to yellow
functional group
hydroxyl
ketone
Quality Level
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Application
2-（羟甲基）蒽甲苯（可光除去的保护基团）可用于化学笼合（Z)-11-十六烷-1-醇（二点螟性信息素）。
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)
T Janáky et al.
Proceedings of the National Academy of Sciences of the United States of America, 89(21), 10203-10207 (1992-11-01)
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
Man-Yuan Wang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 31(4), 307-308 (2006-05-19)
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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