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线性分子式:
(C6H5CH2)2O
化学文摘社编号:
分子量:
198.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-118-2
Beilstein/REAXYS Number:
1911156
MDL number:
产品名称
二苄醚, purum, ≥98.0% (GC)
InChI key
MHDVGSVTJDSBDK-UHFFFAOYSA-N
InChI
1S/C14H14O/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2
SMILES string
C(OCc1ccccc1)c2ccccc2
grade
purum
assay
≥98.0% (GC)
form
liquid
refractive index
n20/D 1.562
bp
158-160 °C/10 mmHg (lit.)
mp
1.5-3.5 °C (lit.)
density
1.043 g/mL at 20 °C (lit.)
functional group
ether
phenyl
Quality Level
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Application
- 绿色合成路径:研究采用二苄醚制备苄基苯基硫醚的绿色合成路径,意在通过环境友好方法进行化学合成(Wu et al., 2023)。
- 热解合成纳米颗粒:采用二苄醚通过热解反应合成氧化锰纳米颗粒,说明它可促进受控化学反应(Martinez de la Torre and Bennewitz, 2020)。
General description
已研究二苄基醚在水溶液中的热分解反应,探讨煤在超临界水中反应生成的挥发物。测定了二苄基醚在 CO 2 和乙醇混合物中的无限稀释扩散系数。
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1B
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
278.6 °F - Pensky-Martens closed cup
flash_point_c
137 °C - Pensky-Martens closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Dibenzyl ether as a probe into the supercritical fluid solvent extraction of volatiles from coal with water.
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Diffusion of benzyl acetate, 2-phenylethyl acetate, 3-phenylpropyl acetate, and dibenzyl ether in mixtures of carbon dioxide and ethanol.
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G A Burdock et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 30(7), 559-566 (1992-07-01)
Dibenzyl ether (FEMA No. 2371, CAS No. 103-50-4) was given in the diet to rats at a rate of 62, 196 or 620 mg/kg/day for 91 consecutive days. Body weights and food consumption were measured weekly; haematological, clinical chemistry and
E Zimerson et al.
Contact dermatitis, 43(2), 72-78 (2000-08-17)
In patients hypersensitive to p-tert-butylphenol-formaldehyde resin (PTBP-F-R), it is for diagnostic, therapeutic and preventive reasons necessary to know the identity of the primary sensitizing substances, their sensitizing capacities as well as their cross-reaction patterns. We have recently shown that the
Hosamani Basavaprabhu et al.
Organic & biomolecular chemistry, 10(13), 2528-2533 (2012-03-01)
An application of the classical Ritter reaction for the synthesis of unsymmetrical di and trisubstituted ureas catalyzed by FeCl(3) is described. The protocol is of significant interest in view of the easy availability of precursors, mild reaction conditions employed and
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