38490
5,5-二甲基-1,3-环己二酮
derivatization grade (HPLC), for the determination of aldehyde formaldehyde, ≥99.0%
别名:
双甲酮, 甲酮
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关于此项目
线性分子式:
(CH3)2C6H6(=O)2
化学文摘社编号:
分子量:
140.18
UNSPSC Code:
12164500
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-804-4
Beilstein/REAXYS Number:
471489
MDL number:
产品名称
5,5-二甲基-1,3-环己二酮, derivatization grade (HPLC), for the determination of aldehyde formaldehyde, ≥99.0%
InChI key
BADXJIPKFRBFOT-UHFFFAOYSA-N
InChI
1S/C8H12O2/c1-8(2)4-6(9)3-7(10)5-8/h3-5H2,1-2H3
SMILES string
CC1(C)CC(=O)CC(=O)C1
grade
derivatization grade (HPLC)
assay
≥99.0% (GC)
≥99.0%
quality
for the determination of aldehyde formaldehyde
mp
146-148 °C (lit.)
application(s)
general analytical
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Jesse C Patterson et al.
Cell systems, 8(2), 163-167 (2019-02-25)
Although elevated levels of reactive oxygen species (ROS) have been observed in cancer cells and cancer cells aberrantly proliferate, it is not known whether the level of reactive oxygen species and the accumulation of oxidative damage to macromolecules vary across
Trace analysis of aldehydes by reversed-phase high-performance liquid chromatography and precolumn fluorigenic labeling with 5, 5-dimethyl-1, 3-cyclohexanedione.
Kenneth M
Journal of Chromatography A, 256, 243-252 (1983)
Solid-State Condensation Reactions Between Aldehydes and 5, 5-Dimethyl-1, 3-cyclohexanedione by Grinding at Room Temperature.
Tong-shou J
Synthetic Communications, 35 (17), 2339-2345 (2005)
Condensation of aromatic aldehydes with 5, 5-dimethyl-1, 3-cyclohexanedione without catalyst.
Shujiang Tu
Synthetic Communications, 32 (19), 3063-3067 (2002)
Patrick M Dansette et al.
Chemical research in toxicology, 23(7), 1268-1274 (2010-06-19)
Metabolic activation of the tetrahydro-thienopyridine antithrombotic prodrug, prasugrel, involves two steps: an esterase-dependent hydrolysis of its acetate function leading to thiolactone 6 and a cytochrome P450 (P450)-catalyzed oxidative cleavage of this thiolactone. This article shows that this second step involves
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