C101400
1,2-Cyclohexanedione
97%
Synonym(s):
1,2-Dioxocyclohexane, Cyclohexan-1,2-dione
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All Photos(3)
About This Item
Linear Formula:
C6H8(=O)2
CAS Number:
Molecular Weight:
112.13
Beilstein:
507419
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
solid
bp
193-195 °C (lit.)
mp
34-38 °C (lit.)
storage temp.
2-8°C
SMILES string
O=C1CCCCC1=O
InChI
1S/C6H8O2/c7-5-3-1-2-4-6(5)8/h1-4H2
InChI key
OILAIQUEIWYQPH-UHFFFAOYSA-N
Gene Information
human ... ACHE(43) , BCHE(590) , CES1(1066)
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Application
Specific reagent for arginine residues.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
No data available
Flash Point(C)
No data available
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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I Heiland et al.
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The primary structure of protein L21 from the 50S subunit of Escherichia coli ribosomes has been completely determined by sequencing the peptides obtained by digestion of L21 with trypsin before and after modification of the arginine residues with 1,2-cyclohexanedione, Staphylococcus
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The Biochemical journal, 298 ( Pt 2), 295-301 (1994-03-01)
The presence of arginine at the active site of Leishmania donovani adenosine kinase was studied by chemical modification, followed by the characterization of the modified enzyme. The arginine-specific reagents phenylglyoxal (PGO), butane-2,3-dione and cyclohexane-1,2-dione all irreversibly inactivated the enzyme. In
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The homologous lipases from Rhizomucor miehei and Humicola lanuginosa showed approximately the same enantioselectivity when 2-methyldecanoic acid esters were used as substrates. Both lipases preferentially hydrolyzed the S-enantiomer of 1-heptyl 2-methyldecanoate (R. miehei: ES = 8.5; H. lanuginosa: ES =
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