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.)
functional group
amine
oxime
phenyl
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
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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
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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