1,2-Cyclohexanedione
- CAS No.
- 765-87-7
- Chemical Name:
- 1,2-Cyclohexanedione
- Synonyms
- Cyclohexane-1,2-dione;1,2-CYCLOHEXANDIONE;Cyclohexane-1,2-dione 98%;AKOS 197;1,2-CycL;AI3-25042;NSC 32950;CCRIS 6296;BRN 0507419;DIHYDROCATECHOL
- CBNumber:
- CB7854271
- Molecular Formula:
- C6H8O2
- Molecular Weight:
- 112.13
- MOL File:
- 765-87-7.mol
- MSDS File:
- SDS
- Modify Date:
- 2025/1/27 9:38:02
Melting point | 34-38 °C (lit.) |
---|---|
Boiling point | 193-195 °C (lit.) |
Density | 1,118 g/cm3 |
FEMA | 3458 | 2-HYDROXY-2-CYCLOHEXEN-1-ONE |
refractive index | 1.518-1.52 |
Flash point | 184 °F |
storage temp. | 2-8°C |
solubility | Soluble in DMSO |
form | Liquid After Melting |
color | Clear yellow |
Odor | at 10.00 % in dipropylene glycol. sweet acorn nut skin maple caramel brothy |
Odor Type | nutty |
Water Solubility | Soluble |
JECFA Number | 424 |
BRN | 507419 |
LogP | 0.252 (est) |
CAS DataBase Reference | 765-87-7(CAS DataBase Reference) |
NIST Chemistry Reference | c-hexane-1,2-dione(765-87-7) |
EPA Substance Registry System | 1,2-Cyclohexanedione (765-87-7) |
1,2-Cyclohexanedione price More Price(4)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich(India) | C101400 | 1,2-Cyclohexanedione 97% | 765-87-7 | 1G | ₹1948.5 | 2022-06-14 | Buy |
Sigma-Aldrich(India) | C101400 | 1,2-Cyclohexanedione 97% | 765-87-7 | 5G | ₹5986.23 | 2022-06-14 | Buy |
TCI Chemicals (India) | C0728 | 1,2-Cyclohexanedione min. 97.0 % | 765-87-7 | 5G | ₹5600 | 2022-05-26 | Buy |
TCI Chemicals (India) | C0728 | 1,2-Cyclohexanedione min. 97.0 % | 765-87-7 | 25G | ₹19500 | 2022-05-26 | Buy |
1,2-Cyclohexanedione Chemical Properties,Uses,Production
Chemical Properties
clear yellow liquid after melting
Uses
1,2-Cyclohexanedione have been used as a substrate to study enzyme cyclohexane-1,2-dione hydrolase as a new tool to degrade alicyclic compounds.
Reactions
1,2-Cyclohexanedione may effectively occupy vacant coordination sites and thus promote the present cycloisomerization[1]. Tanaka et al. research the catalytic cycloisomerization of 1,6- and 1,7-diynes leading to trienes and vinylpyrroles by using a cationic rhodium(I)/Segphos complex (2.5-10 mol %) and 1,2-cyclohexanedione (100 mol %).
Synthesis Reference(s)
Journal of the American Chemical Society, 73, p. 4658, 1951 DOI: 10.1021/ja01154a048
Tetrahedron Letters, 25, p. 603, 1984 DOI: 10.1016/S0040-4039(00)99949-0
The Journal of Organic Chemistry, 39, p. 3295, 1974 DOI: 10.1021/jo00936a034
References
[1] Ken Tanaka, Masao Hirano, Yousuke Otake. “Cationic Rhodium(I)/Segphos-Catalyzed Cycloisomerization of 1,6- and 1,7-Diynes in the Presence of 1,2-Cyclohexanedione.” Organic Letters 9 20 (2007): 3953–3956.
1,2-Cyclohexanedione Preparation Products And Raw materials
Raw materials
Preparation Products
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Supplier | Advantage |
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GLR Innovations | 58 |
Firmus Laboratories Pvt Ltd | 58 |
DHANVI EXIM SERVICES | 58 |
V & V Pharma Industries | 58 |
S. Nihar Exports | 50 |
Alfa Aesar | 58 |
5 E Scientific | 58 |
OCEAN TRADING CORPORATION | 58 |
CHEMSWORTH | 30 |
TCI Chemicals (India) Pvt. Ltd. | 58 |
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