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330256

Sigma-Aldrich

4′-Hydroxy-3′-nitroacetophenone

98%

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5 ML
CN¥1,175.99
25 ML
CN¥4,218.89

CN¥1,175.99


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5 ML
CN¥1,175.99
25 ML
CN¥4,218.89

About This Item

Linear Formula:
HOC6H3(NO2)COCH3
CAS Number:
Molecular Weight:
181.15
Beilstein:
1959078
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

CN¥1,175.99


In StockDetails


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Assay

98%

form

solid

mp

132-135 °C (lit.)

functional group

ketone
nitro

SMILES string

CC(=O)c1ccc(O)c(c1)[N+]([O-])=O

InChI

1S/C8H7NO4/c1-5(10)6-2-3-8(11)7(4-6)9(12)13/h2-4,11H,1H3

InChI key

MMNKVWGVSHRIJL-UHFFFAOYSA-N

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This Item
P9416P228793773
technique(s)

blocking: suitable, hybridization: suitable, transformation: suitable, cell culture | mammalian: suitable, protein purification: suitable

technique(s)

-

technique(s)

cell culture | mammalian: suitable

technique(s)

DNA extraction: suitable, RNA extraction: suitable, cell culture | mammalian: suitable, protein purification: suitable

form

viscous liquid

form

viscous liquid

form

viscous liquid

form

viscous liquid

biological source

plant

biological source

corn, plant (Palm), plant (coconut), wheat

biological source

-

biological source

-

CMC

0.06 mM (20-25°C)

CMC

60 mg/L

CMC

0.06 mM (20-25°C)

CMC

-

transition temp

cloud point 76 °C

transition temp

-

transition temp

cloud point 76 °C

transition temp

-

cation traces

Al: ≤0.0005%, Cu: ≤0.0005%, K: ≤0.005%, NH4+: ≤0.05%, Pb: ≤0.001%, Ca: ≤0.0005%, Mg: ≤0.0005%, Zn: ≤0.0005%, Fe: ≤0.0005%, Na: ≤0.05%

cation traces

-

cation traces

-

cation traces

-

Application

4′-Hydroxy-3′-nitroacetophenone may be used in chemical synthesis.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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Iron-catalyzed cross-coupling of primary and secondary alkyl halides with aryl grignard reagents.
Nakamura M
Journal of the American Chemical Society, 126(12), 3686-3687 (2004)
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Investigation of the essential oil of the aerial parts of Eryngium maritimum L. from Corsica led to the isolation of one known sesquiterpene (1) and three new oxygenated sesquiterpenes with a muurolane or cadinane skeleton (2-4). Structure assignments of 4
Kai Sotthewes et al.
Langmuir : the ACS journal of surfaces and colloids, 29(11), 3662-3667 (2013-02-21)
The energetics and dynamics of the various phases of decanethiolate self-assembled monolayers on Au(111) surfaces were studied with scanning tunneling microscopy. We have observed five different phases of the decanethiolate monolayer on Au(111): four ordered phases (β, δ, χ*, and
Ilya V Pobelov et al.
Journal of physics. Condensed matter : an Institute of Physics journal, 24(16), 164210-164210 (2012-04-03)
We describe a new setup for simultaneous measurements of force and current in conductive nanocontacts in a liquid environment with a high sampling rate and resolution. A lab-built current-to-voltage converter allows measurements of the current over seven orders of magnitude.

Protocols

Separation of Decane; Dodecane; Tetradecane; Hexadecane; Octadecane; Eicosane; Docosane; Tetracosane; Hexacosane; Octacosane

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