W354805
2′-羟基苯乙酮
≥98%
别名:
2-乙酰苯酚
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关于此项目
线性分子式:
HOC6H4COCH3
化学文摘社编号:
分子量:
136.15
FEMA Number:
3548
Council of Europe no.:
4136
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
7.124
EC Number:
204-288-0
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
386123
Organoleptic:
hawthorne; herbaceous; phenolic; sweet
Grade:
Fragrance grade
Biological source:
synthetic
Agency:
follows IFRA guidelines, meets purity specifications of JECFA
Food allergen:
no known allergens
SMILES string
CC(=O)c1ccccc1O
InChI
1S/C8H8O2/c1-6(9)7-4-2-3-5-8(7)10/h2-5,10H,1H3
InChI key
JECYUBVRTQDVAT-UHFFFAOYSA-N
biological source
synthetic
grade
Fragrance grade
agency
follows IFRA guidelines, meets purity specifications of JECFA
reg. compliance
EU Regulation 1223/2009
vapor density
4.7 (vs air)
vapor pressure
~0.2 mmHg ( 20 °C)
assay
≥98%
Quality Level
bp
213 °C/717 mmHg (lit.)
mp
3-6 °C (lit.)
density
1.133 g/mL at 20 °C, 1.131 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
fragrance allergen
no known allergens
organoleptic
hawthorne; herbaceous; phenolic; sweet
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存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
222.8 °F - closed cup
flash_point_c
106 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Xiao-Feng Wu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(40), 12595-12598 (2012-08-29)
Flavone of the month: a general and efficient method for the palladium-catalyzed carbonylative synthesis of flavones has been developed. Starting from aryl bromides and 2-hydroxyacetophenones, the corresponding flavones have been isolated in good yields.
Daniele Gabriel et al.
Journal of cardiovascular pharmacology, 57(1), 20-27 (2011-01-15)
Isatin (1H-indole-2,3 dione) is an endogenous compound with biological activities. Many of its derivatives have pharmacological effects, including inhibition of cyclic guanosine monophosphate levels in cardiac tissue; sedative-hypnotic profiles; anticonvulsant, analgesic, antithermic, and anti-inflammatory activities; and anxiolytic, antimicrobial, and proapoptotic
Nora H Al-Shaalan
Molecules (Basel, Switzerland), 16(10), 8629-8645 (2011-10-15)
The Schiff base hydrazone ligand HL was prepared by the condensation reaction of 7-chloro-4-quinoline with o-hydroxyacetophenone. The ligand behaves either as monobasic bidentate or dibasic tridentate and contain ONN coordination sites. This was accounted for be the presence in the
Mohammed Y Merza et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(7), 1677-1683 (2004-05-19)
Ultra violet absorption spectra of o-methylacetophenone, o-fluoroacetophenone and o-hydroxyacetophenone solutions in different solvents are recorded in the region 200-350 nm at room temperature. Excited state dipole moments for three (pi* <-- pi) transitions of the benzene ring for solutions in
R R Zaky et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 28-34 (2011-07-26)
Schiff base complexes of Cu(II), Ni(II) and Zn(II) with the o-hydroxyacetophenone [N-(3-hydroxy-2-naphthoyl)] hydrazone (H(2)o-HAHNH) containing N and O donor sites have been synthesized. Both ligand and its metal complexes were characterized by different physicochemical methods, elemental analysis, molar conductivity ((1)H
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