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Key Documents

647659

Sigma-Aldrich

Acetophenone oxime

95%

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About This Item

Empirical Formula (Hill Notation):
C8H9NO
CAS Number:
Molecular Weight:
135.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

solid

bp

118-120 °C/20 mmHg (lit.)

mp

55-60 °C (lit.)

density

1.11 g/mL at 25 °C (lit.)

storage temp.

−20°C

SMILES string

C\C(=N/O)c1ccccc1

InChI

1S/C8H9NO/c1-7(9-10)8-5-3-2-4-6-8/h2-6,10H,1H3/b9-7+

InChI key

JHNRZXQVBKRYKN-VQHVLOKHSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Tomasz Kosmalski et al.
ChemistryOpen, 7(7), 551-557 (2018-08-02)
In this study, we present a convenient method for the synthesis of oxime ethers by reacting oximes with various chlorides (alkyl, functionalized alkyl, and benzyl) and with the subsequent use of a super base-pulverized potassium hydroxide in DMSO. The reactions
Rajkumar Kore et al.
Dalton transactions (Cambridge, England : 2003), 47(23), 7795-7803 (2018-06-01)
Two solids of differing Lewis acidities, triethylammonium tetrachlorozincate ([HN222]2[ZnCl4]) and AlCl3, have been combined across 0.1 to 0.9 mole fractions (with respect to [HN222]2[ZnCl4]), and homogeneous solid double salts or mixed metal [HN222]2x[(1 - x)AlCl3 + xZnCl4] double salt ionic

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