10872
3-Chloro-2,4-pentanedione
≥97.0% (GC)
Synonym(s):
3-Cl-ACAC, 3-Chloroacetylacetone
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About This Item
Linear Formula:
CH3COCHClCOCH3
CAS Number:
Molecular Weight:
134.56
EC Number:
216-902-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
605870
MDL number:
assay
≥97.0% (GC)
manufacturer/tradename
Wacker Chemie AG
refractive index
n20/D 1.483 (lit.)
bp
49-52 °C/18 mmHg (lit.)
density
1.1921 g/mL at 20 °C (lit.)
SMILES string
CC(=O)C(Cl)C(C)=O
InChI
1S/C5H7ClO2/c1-3(7)5(6)4(2)8/h5H,1-2H3
InChI key
VLRGXXKFHVJQOL-UHFFFAOYSA-N
General description
3-chloro-2,4-pentanedione undergoes catalytic reduction with electrogenerated cobalt(I)salen via one-electron transfer to form 2,4-pentanedion-3-ate. It forms bis(3-chloro-2,4-pentanedionato)copper complex with copper.
Other Notes
prices for bulk quantities on request
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
132.8 °F - closed cup
flash_point_c
56 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Structural features of homo-and heteroleptic complexes of copper (II) with 2, 2, 6, 6-tetramethyl-3, 5-heptanedione and 3-chloro-2, 4-pentanedione.
Sans-Lenain S and Gleizes A.
Inorgorganica Chimica Acta, 211(1), 67-75 (1993)
M J Samide et al.
Journal of pharmaceutical and biomedical analysis, 19(1-2), 193-203 (2000-03-04)
We have studied the catalytic two-electron reduction of 3-chloro-2,4-pentanedione by cobalt(I) salen electrogenerated at a glassy carbon cathode in acetonitrile containing tetramethylammonium tetrafluoroborate. When cobalt(I) salen is electrogenerated at -0.65 V (a potential that is 30 mV more negative than
Almeqdad Y Habashneh et al.
Archiv der Pharmazie, 347(6), 415-422 (2014-03-13)
A new series of N1-(flavon-6-yl)amidrazones were synthesized by reacting the hydrazonoyl chloride derived from 6-aminoflavone with the appropriate sec-cyclic amines. The antitumor activities of these compounds were evaluated on breast cancer (MCF-7) and leukemic (K562) cell lines. Among the compounds
Jennifer A Jacobsen et al.
Journal of medicinal chemistry, 54(2), 591-602 (2010-12-30)
Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced hit rates ranging from 29% to 43% for five matrix metalloproteases
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 440442-5G | 04061836826949 |
| 440442-1G | 04061836826932 |
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