3-CHLORO-2,4-PENTANEDIONE
Names
[ CAS No. ]:
1694-29-7
[ Name ]:
3-CHLORO-2,4-PENTANEDIONE
[Synonym ]:
3-Chloroacetylacetone
3-Chloropentane-2,4-dione
EINECS 216-902-4
MFCD00009651
Chemical & Physical Properties
[ Density]:
1.129 g/mL at 25 °C(lit.)
[ Boiling Point ]:
49-52 °C18 mm Hg(lit.)
[ Melting Point ]:
-15 °C
[ Molecular Formula ]:
C5H7ClO2
[ Molecular Weight ]:
134.56100
[ Flash Point ]:
54 °F
[ Exact Mass ]:
134.01300
[ PSA ]:
34.14000
[ LogP ]:
0.77180
[ Vapour Pressure ]:
0.0215mmHg at 25°C
[ Index of Refraction ]:
n20/D 1.483(lit.)
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Symbol ]:
GHS02, GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H226-H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
36/37/38
[ Safety Phrases ]:
S26
[ RIDADR ]:
UN 1224 3/PG 3
[ WGK Germany ]:
3
[ Packaging Group ]:
II
[ Hazard Class ]:
3.1
[ HS Code ]:
2914700090
Synthetic Route
Customs
[ HS Code ]: 2914700090
[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%
Articles
J. Med. Chem. 54 , 591-602, (2011)
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...
Electrochemical behavior of 3-chloro-2,4-pentanedione in the presence of cobalt salen.J. Pharm. Biomed. Anal. 19(1-2) , 193-203, (1999)
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 tetraflu...
Synthesis and antitumor activities of some new N1-(flavon-6-yl)amidrazone derivatives.Arch. Pharm. (Weinheim) 347(6) , 415-22, (2014)
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 ...