P16621
苯乙酸
99%
别名:
α-甲苯甲酸, α-甲苯酸, 聚丙烯酰胺, 苯乙酸
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关于此项目
线性分子式:
C6H5CH2CO2H
化学文摘社编号:
分子量:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-148-6
Beilstein/REAXYS Number:
1099647
MDL number:
产品名称
苯乙酸, 99%
InChI key
WLJVXDMOQOGPHL-UHFFFAOYSA-N
InChI
1S/C8H8O2/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)
SMILES string
OC(=O)Cc1ccccc1
vapor density
~4 (vs air)
vapor pressure
1 mmHg ( 97 °C)
assay
99%
form
crystals
bp
265 °C (lit.)
mp
76-78 °C (lit.)
density
1.081 g/mL at 25 °C (lit.)
Quality Level
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Application
- Phenylacetic acid can be used to synthesize a variety of phenyl substituted compounds by Pd (II)-catalyzed C-H activation/aryl-aryl coupling reaction.
- It can be employed in the preparation of Mn16 single-molecule magnets by reductive aggregation route.
- It can be used as a precursor to synthesize chromones, isoflavones, and homoisoflavones.
- It can also be used as a key precursor in the synthesis of emethallicin E and (−)-incarviatone A.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
269.6 °F - closed cup
flash_point_c
132 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Versatile Pd (II)-Catalyzed C? H Activation/Aryl? Aryl Coupling of Benzoic and Phenyl Acetic Acids.
Wang D H, et al.
Journal of the American Chemical Society, 130(52), 17676-17677 (2008)
Enantioselective Total Synthesis of (?)-Incarviatone A.
Hong B, et al.
Journal of the American Chemical Society, 137(37), 11946-11949 (2015)
Synthesis and biological evaluation of epidithio-, epitetrathio-, and bis-(methylthio) diketopiperazines: synthetic methodology, enantioselective total synthesis of epicoccin G, 8, 8?-epi-ent-rostratin B, gliotoxin, gliotoxin G, emethallicin E, and haematocin and discovery of new antiviral and antimalarial agents.
Nicolaou K C, et al.
Journal of the American Chemical Society, 134(41), 17320-17332 (2012)
A Family of Mn16 Single-Molecule Magnets from a Reductive Aggregation Route.
King P, et al.
Inorganic Chemistry, 43(23), 7315-7323 (2004)
A mild and efficient protocol to synthesize chromones, isoflavones, and homoisoflavones using the complex 2, 4, 6-trichloro-1, 3, 5-triazine/dimethylformamide.
Basha G M, et al.
Canadian Journal of Chemistry, 91(8), 763-768 (2013)
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