2-methyl-1,3-cyclohexane dione
1,3-cyclohexanedione, 2-methyl-
Identification
| Name | 2-methyl-1,3-cyclohexane dione |
| IUPAC | 2-methylcyclohexane-1,3-dione |
| CAS Number | 1193-55-1 |
| EINECS | 214-773-9 |
| FDA UNII | Search |
| Molecular Formula | C7 H10 O2 |
| Molecular Weight | 126.15510000 |
| MDL Number | MFCD00001587 |
| Nikkaji Number | J183.672B |
| Beilstein | 1281598 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 235.70 °C. @ 760.00 mm Hg (est) |
| Flash Point | 187.00 °F. TCC ( 85.90 °C. ) (est) |
| logP (o/w) | -0.390 (est) |
| Soluble in | water, 1.794e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for 2-methyl-1,3-cyclohexane dione usage levels up to | not for fragrance use. |
| Recommendation for 2-methyl-1,3-cyclohexane dione flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
1,3-
cyclohexanedione, 2-methyl-
2-
methyl cyclohexane-1,3-dione
2-
methyl-1,3-cyclohexanedione
2-
methylcyclohexane-1,3-dione
PubMed:
Palladium-Catalyzed Cross-Coupling of 2,5-Cyclohexadienyl-Substituted Aryl or Vinylic Iodides and Carbon or Heteroatom Nucleophiles.
PubMed:
Conformational transformation coupled with the order-disorder phase transition in 2-methyl-1,3-cyclohexanedione crystals. erratum
PubMed:
Conformational transformation coupled with the order-disorder phase transition in 2-methyl-1,3-cyclohexanedione crystals.
PubMed:
New initiator system for bonding to dentin using methylcyclohexanedione.
PubMed:
Protection of Escherichia coli against radiation damage by 2-methyl-1,3-cyclohexanedione and some related compounds.