187240
9-蒽甲醇
97%
别名:
9-(羟甲基)蒽
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关于此项目
经验公式（希尔记法）:
C15H12O
化学文摘社编号:
分子量:
208.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-998-5
Beilstein/REAXYS Number:
1873402
MDL number:
产品名称
9-蒽甲醇, 97%
InChI key
JCJNNHDZTLRSGN-UHFFFAOYSA-N
InChI
1S/C15H12O/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9,16H,10H2
SMILES string
OCc1c2ccccc2cc3ccccc13
assay
97%
solubility
chloroform: soluble 20 mg/mL, clear to slightly hazy, light yellow to yellow
functional group
hydroxyl
Quality Level
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Application
9-蒽甲醇可用于：
- 作为制备9-蒽甲基-1-哌嗪羧酸酯的起始原料，充当HPLC测定异氰酸酯的试剂。
- Diels-Alder 反应,与二甲基乙炔-二羧酸酯反应生成内酯衍生物。
- 作为δ-戊内酯开环聚合反应引发剂，合成聚（(δ-戊内酯)。
- 作为合成聚合物载体蒽的起始材料，在环加成反应中充当亲二烯体清除剂。
General description
9-蒽甲醇参与由氧化铝烷催化的L-丙交酯的开环聚合反应。它与叔-丁醇钾发生质子交换反应，生成9-蒽甲醇。
9-蒽甲醇是蒽的衍生物，常用于Diels-Alder反应。
9-蒽甲醇是蒽的衍生物，常用于Diels-Alder反应。
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)
Living cationic polymerization of δ-valerolactone and synthesis of high molecular weight homopolymer and asymmetric telechelic and block copolymer
Lou X, et al.
Macromolecules, 35, 1190-1195 (2002)
Shanshan Kou et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 768-775 (2012-08-14)
Vibrational spectral measurements were made for 9-anthracenemethanol. Optimized geometrical structure and harmonic vibration frequencies were computed based on ab initio and density functional theory B3LYP methods using 6-311G(**) and LANL2DZ basis sets. The equilibrium geometries got from all of the
Cyclodextrin-promoted Diels Alder reactions of a polycyclic aromatic hydrocarbon under mild reaction conditions
Chaudhuri, et al.
Tetrahedron Letters, 56, 1619-1623 (2015)
Development of a new approach for total isocyanate determination using the reagent 9-anthracenylmethyl-1-piperazinecarboxylate.
Roh Y-M, et al.
Analyst, 125(9), 1691-1696 (2000)
Yuzhan Li et al.
Scientific reports, 10(1), 20214-20214 (2020-11-21)
The development of multi-stimuli-responsive shape memory polymers has received increasing attention because of its scientific and technological significance. In this work, epoxy elastomers with reversible crosslinks are synthesized by polymerizing an anthracene-functionalized epoxy monomer, a diepoxy comonomer, and a dicarboxylic
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