2-HYDROXYCYCLOHEXANONE DIMER
2-HYDROXYCYCLOHEXANONE DIMER Basic information
- Product Name:
- 2-HYDROXYCYCLOHEXANONE DIMER
- Synonyms:
-
- Cyclohexanone, 2-hydroxy-, dimer
- 2-HYDROXY-CYCLOHEXANONE
- ADIPOIN
- AKOS 92461
- 2-HYDROXYCYCLOHEXANONE, DIMER, 90+%
- 2-Hydroxycyclohexanone dimer,Adipoin
- NSC 117392
- 2-Hydroxycyclohexanone dimer 98%
- CAS:
- 30282-14-5
- MF:
- C6H10O2
- MW:
- 228.28
- EINECS:
- 621-164-5
- Product Categories:
-
- Building Blocks
- C11 to C12
- Carbonyl Compounds
- Chemical Synthesis
- Ketones
- Organic Building Blocks
- Mol File:
- 30282-14-5.mol
2-HYDROXYCYCLOHEXANONE DIMER Chemical Properties
- Melting point:
- 100-107 °C(lit.)
- Boiling point:
- 83-86 °C13 mm Hg(lit.)
- Flash point:
- 175 °F
- storage temp.
- 2-8°C
- form
- Powder
- color
- Off-white
- Water Solubility
- Partly miscible in water.
Safety Information
- Hazard Codes
- F,Xi
- Risk Statements
- 11-36/37/38
- Safety Statements
- 16-26-36
- RIDADR
- UN 1325 4.1/PG 3
- WGK Germany
- 3
- F
- 9-21
- HazardClass
- 4.1
- PackingGroup
- III
- HS Code
- 29144090
2-HYDROXYCYCLOHEXANONE DIMER Usage And Synthesis
Chemical Properties
Off-white powder
Uses
Reactant involved in:• ;Synthesis of substrated for tin tetrachloride mediated fragmentation to produce ynones and ynoates1• ;Tandem oxidation coupling reactions with diamines2• ;Asymmetric allylic alkylation of enolates3• ;Formate reduction of allylic carbonates for polypropionate systems4
Uses
It is a reactant involved in the synthesis of substrates for tin tetrachloride mediated fragmentation to produce ynones and ynoates, tandem oxidation coupling reactions with diamines, asymmetric allylic alkylation of enolates and formate reduction of allylic carbonates for polypropionate systems.
Uses
Reactant involved in:
- Synthesis of substrated for tin tetrachloride mediated fragmentation to produce ynones and ynoates
- Tandem oxidation coupling reactions with diamines
- Asymmetric allylic alkylation of enolates
- Formate reduction of allylic carbonates for polypropionate systems
Definition
ChEBI: 2-hydroxycyclohexan-1-one is a secondary alpha-hydroxy ketone and a hydroxycyclohexanone.
Synthesis Reference(s)
The Journal of Organic Chemistry, 51, p. 130, 1986 DOI: 10.1021/jo00352a002
Synthetic Communications, 25, p. 3141, 1995 DOI: 10.1080/00397919508015463
Tetrahedron Letters, 36, p. 3031, 1995 DOI: 10.1016/0040-4039(95)00419-D
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