B4856
二苯甲醇
99%
别名:
α-苯基苯甲醇, 二苯基甲醇, 苯甲醇
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关于此项目
线性分子式:
(C6H5)2CHOH
化学文摘社编号:
分子量:
184.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-033-8
Beilstein/REAXYS Number:
1424379
MDL number:
产品名称
二苯甲醇, 99%
InChI key
QILSFLSDHQAZET-UHFFFAOYSA-N
InChI
1S/C13H12O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H
SMILES string
OC(c1ccccc1)c2ccccc2
assay
99%
form
powder
bp
297-298 °C (lit.)
mp
65-67 °C (lit.)
Quality Level
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Application
二苯基甲醇用于卡宾催化的α，α-二取代羧酸酯的动态动力学拆分。也可用于游离碱和 Ni (II) 卟啉配合物的手性拆分。
存储类别
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
Carbene-Catalyzed Dynamic Kinetic Resolution of Carboxylic Esters.
Chen X, et al.
Journal of the American Chemical Society, 138(23), 7212-7215 (2016)
Helimeric porphyrinoids: stereostructure and chiral resolution of meso-tetraarylmorpholinochlorins.
Bru?ckner C, et al.
Journal of the American Chemical Society, 133(22), 8740-8752 (2011)
Alkylation of alcohols for gas chromatographic analysis by a phase transfer catalysis technique. Evaluation of benzhydrol benzylation in a one-phase system.
H Brink et al.
Acta pharmaceutica Suecica, 16(4), 247-262 (1979-01-01)
Xiao-Dong Ma et al.
Bioorganic & medicinal chemistry, 19(16), 4704-4709 (2011-07-27)
A series of (±)-benzhydrol derivatives featuring the essential sulfonamide group at the para position on the C-ring were synthesized and evaluated for the potential anti-HIV activity in C8166 cells. Most of these analogues demonstrated low concentration inhibitory activity with EC(50)
Masanori Ichikawa et al.
Bioorganic & medicinal chemistry, 20(9), 3072-3093 (2012-04-03)
In the present article, we have reported the design, synthesis, and identification of highly potent benzhydrol derivatives as squalene synthase inhibitors (compound 1). Unfortunately, the in vivo efficacies of the compounds were not enough for acquiring the clinical candidate. We
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