1,3-Cyclohexanedione, 4,4,6,6-tetramethyl-

Base Information

Chemical Name:1,3-Cyclohexanedione, 4,4,6,6-tetramethyl-
CAS No.:60681-10-9
Molecular Formula:C₁₀H₁₆O₂
Molecular Weight:168.236
Hs Code.:
DSSTox Substance ID:DTXSID60209496
Wikidata:Q83083800

Synonyms:1,3-Cyclohexanedione, 4,4,6,6-tetramethyl-;60681-10-9;1,3-Cyclohexanedione,4,4,6,6-tetramethyl-;SCHEMBL2607982;DTXSID60209496

Suppliers and Price of 1,3-Cyclohexanedione, 4,4,6,6-tetramethyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 1,3-Cyclohexanedione, 4,4,6,6-tetramethyl-

Chemical Property:

Vapor Pressure:0.0282mmHg at 25°C
Boiling Point:245.8°C at 760 mmHg
Flash Point:90.1°C
Density:0.954g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:168.115029749
Heavy Atom Count:12
Complexity:212

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CC(C(=O)CC1=O)(C)C)C

Technology Process of 1,3-Cyclohexanedione, 4,4,6,6-tetramethyl-

There total 3 articles about 1,3-Cyclohexanedione, 4,4,6,6-tetramethyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%

: 81887-88-9
2-Diazo-3-hydroxy-4,4,6,6-tetramethyl-1-cyclohexanone

: 60681-10-9
4,4,6,6-Tetramethyl-cyclohexane-1,3-dione

: 81887-98-1
2,2,4,4-Tetramethyl-5-oxo-cyclopentanecarbaldehyde

Guidance literature:: With sulfuric acid; In tetrahydrofuran; water; at 18 - 20 ℃; for 5.5h; Product distribution; Mechanism;

Reference yield:

: 4694-11-5
2,2,4,4-tetramethylcyclopentanone

: 60681-10-9
4,4,6,6-Tetramethyl-cyclohexane-1,3-dione

Guidance literature:: Multi-step reaction with 2 steps

1: SeO₂ / dioxane

2: aq. KOH / diethyl ether

With potassium hydroxide; selenium(IV) oxide; In 1,4-dioxane; diethyl ether;