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线性分子式:
CH3COC6H5
化学文摘社编号:
分子量:
120.15
UNSPSC Code:
12352100
PubChem Substance ID:
eCl@ss:
39023804
EC Number:
202-708-7
Beilstein/REAXYS Number:
605842
MDL number:
InChI key
KWOLFJPFCHCOCG-UHFFFAOYSA-N
InChI
1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3
SMILES string
CC(=O)c1ccccc1
vapor density
4.1 (vs air)
vapor pressure
0.45 mmHg ( 25 °C), 1 mmHg ( 15 °C)
assay
≥98.0% (GC)
autoignition temp.
1058 °F
bp
202 °C (lit.)
mp
19-20 °C (lit.)
density
1.03 g/mL at 25 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
179.6 °F - closed cup
flash_point_c
82 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Comment on "closing the loop on bond selective chemistry using tailored strong field laser pulses".
Xin Zhu et al.
The journal of physical chemistry. A, 113(17), 5264-5266 (2009-04-24)
Effects of solvent and substituents on the absorption spectra of triplet acetophenone and the acetophenone ketyl radical studied by nanosecond laser photolysis.
Lutz H, et al.
The Journal of Physical Chemistry, 77(14), 1758-1762 (1973)
Optically active nitrogen ligans: III. Enantioface-discriminating transfer hydrogenation of acetophenone catalyzed by rhodium (I) complexes with chiral 2-(2'-pyridyl) pyridines.
Botteghi C, et al.
Journal of Organometallic Chemistry, 304(1), 217-225 (1986)
Enantioselective hydrosilylation of acetophenone with rhodium/oxazolines catalysts.
Balavoine G, et al.
Tetrahedron Letters, 30(38), 5141-5144 (1989)
Ohmori N, et al.
The Journal of Physical Chemistry, 92(5), 1086-1093 (1988)
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