B99006
2-仲丁基苯酚
98%
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关于此项目
线性分子式:
C2H5CH(CH3)C6H4OH
化学文摘社编号:
分子量:
150.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-933-8
Beilstein/REAXYS Number:
1210026
MDL number:
Assay:
98%
Form:
liquid
SMILES string
CCC(C)c1ccccc1O
InChI
1S/C10H14O/c1-3-8(2)9-6-4-5-7-10(9)11/h4-8,11H,3H2,1-2H3
InChI key
NGFPWHGISWUQOI-UHFFFAOYSA-N
vapor pressure
0.03 mmHg ( 20 °C)
assay
98%
form
liquid
Quality Level
Gene Information
rat ... Ar(24208)
refractive index
n20/D 1.522 (lit.)
bp
226-228 °C (lit.)
mp
12 °C (lit.)
density
0.982 g/mL at 25 °C (lit.)
Application
2-sec-Butylphenol is a precursor to synthesize various coumarin and benzofuran derivatives that are used as lipid-lowering agents and potential bone anabolic agents. It can also be used as a solvent in organic synthesis.
signalword
Danger
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 2
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
法规信息
新产品
此项目有
Benzofuran-pyran hybrids: A new class of potential bone anabolic agents.
Gupta S, et al.
Bioorganic & Medicinal Chemistry Letters, 28(10), 1719-1724 (2018)
V P Bintoro et al.
The Analyst, 120(11), 2747-2753 (1995-11-01)
A rapid, simple and direct visible spectrophotometric method, based on the quantitative nitration of 2-sec-butylphenol in concentrated sulfuric acid, is described for the determination of nitrate in milk. The nitration product was extracted into toluene and the yellow nitrophenoxide compound
Masashi Hattori et al.
Physical chemistry chemical physics : PCCP, 19(5), 3688-3693 (2017-01-18)
Photo-assisted phosphorylation of an anatase TiO
RuSn bimetallic catalysts for selective hydrogenation of levulinic acid to ?-valerolactone.
Wettstein S G, et al.
Applied Catalysis. B, Environmental, 117, 321-329 (2012)
Discovery of coumarin?dihydropyridine hybrids as bone anabolic agents.
Sashidhara K V, et al.
Journal of Medicinal Chemistry, 56(1), 109-122 (2012)
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