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![(2R)-2-Phenyl-3,4-dihydro-2H-pyrimido[2,1-b][1,3]benzothiazole ≥95%](/deepweb/assets/sigmaaldrich/product/structures/302/833/59a06b8b-9e9d-4dc4-a4ed-a36ab5081792/640/59a06b8b-9e9d-4dc4-a4ed-a36ab5081792.png)
品質等級
化驗
99%
形狀
liquid
折射率
n20/D 1.573 (lit.)
bp
138 °C/9 mmHg (lit.)
密度
1.436 g/mL at 25 °C (lit.)
官能基
bromo
hydroxyl
SMILES 字串
OCCc1ccc(Br)cc1
InChI
1S/C8H9BrO/c9-8-3-1-7(2-4-8)5-6-10/h1-4,10H,5-6H2
InChI 密鑰
PMOSJSPFNDUAFY-UHFFFAOYSA-N
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應用
4-Bromophenethyl alcohol was used in the synthesis of 4-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenethoxy)quinazoline.
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B Latli et al.
Chemical research in toxicology, 9(2), 445-450 (1996-03-01)
Two candidate photoaffinity probes are designed from 4-substituted quinazolines known to be potent insecticides/acaricides and NADH:ubiquinone oxidoreductase inhibitors acting at or near the rotenone site. 4-(11-Azidoundecyl-2-amino)quinazoline, based on the undecylamino analog SAN 548A as a prototype, was synthesized in 18%
Roman S Borisov et al.
Talanta, 200, 31-40 (2019-05-01)
This work highlights the discovered in-situ analytical reaction between primary/secondary alcohols and nitrogenous bases (pyridine, quinoline) that involves the substitution of hydroxyl groups for nitrogen-containing charged species and proceeds in an ionization region of Direct Analysis in Real Time mass
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