1,3-Dibenzoylacetone

Suppliers

Names

[ Name ]:
1,3-Dibenzoylacetone

[Synonym ]:
1,3-Dibenzoylacetone
1,3,5-Pentanetrione,1,5-diphenyl
1,3,5-trione
Acetone,s-dibenzoyl
2-Propanone,1,3-dibenzoyl
1,5-Diphenyl-1,3,5-pentanetrione
1,5-diphenylpentan-1,3,5-trione
1,5-diphenyl-1,3,5-penatnetrione
1,5-diphenyl-pentane-1,3,5-trione

Chemical & Physical Properties

[ Density]:
1.172g/cm3

[ Boiling Point ]:
422.7ºC at 760mmHg

[ Melting Point ]:
107-109ºC

[ Molecular Formula ]:
C₁₇H₁₄O₃

[ Molecular Weight ]:
266.29100

[ Flash Point ]:
182.6ºC

[ Exact Mass ]:
266.09400

[ PSA ]:
51.21000

[ LogP ]:
3.10150

[ Vapour Pressure ]:
9.37E-08mmHg at 25°C

[ Index of Refraction ]:
1.574

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2914399090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2914399090

[ Summary ]:
2914399090. other aromatic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Some novel triorganotin(IV) derivatives of β,δ-triketones. Kumar A, et al.

Polyhedron 2(9) , 907-916, (1983)

Reactions of metal ions with triketones. Part 2. Kinetics and mechanisms of the reactions of nickel (II) and cobalt (II) with heptane-2, 4, 6-trione in methanol-water (70: 30 v/v). Hynes MJ and Walsh J.

J. Chem. Soc., Dalton Trans. 12 , 2565-2569, (1985)

Structure and magnetism of a binuclear 1, 3, 5-triketonate complex of cobalt (II), bis (1, 5-diphenyl-1, 3, 5-pentanetrionate) tetrapyridinedicobalt (II) tetrapyridine. Kuszaj JM, et al.

Inorg. Chem. 12(6) , 1297-1303, (1973)

1,3-BIS(PHENYLMETHYL)-2-(2-THIENYL)-IMIDAZOLIDINE
1,3-PROPANEDIONE, 1-(5-CHLORO-2-HYDROXY-3-NITROPHENYL)-3-(4-CHLOROPHENYL)-
1-(3-Methoxyphenyl)-1H-pyrazole-4-carboxylicacid
1,3-PROPANEDIONE, 1-(5-CHLORO-2-HYDROXY-3-NITROPHENYL)-3-(4-NITROPHENYL)-
1,3-Difluoropropan-2-amine
1,3-Adamantanediol dimethacrylate
3-[5-({[(4-ethoxyphenyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]-N-[(furan-2-yl)methyl]propanamide
3-[5-({[(2,5-dimethoxyphenyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]-N-[(furan-2-yl)methyl]propanamide
2-[(5-chloro-2-methoxyphenyl)amino]-2-oxoethyl 4-(1,1-dioxido-2H-1,2,4-benzothiadiazin-3-yl)-3,3-dimethylbutanoate
4-((2-(5-chloro-2-methylphenyl)-1,1-dioxido-3-oxo-2H-benzo[e][1,2,4]thiadiazin-4(3H)-yl)methyl)benzonitrile
2-(5-chloro-2-methylphenyl)-4-(2,5-dimethylbenzyl)-2H-1,2,4-benzothiadiazin-3(4H)-one 1,1-dioxide
N-cyclohexyl-3-[5-({[(3-methoxyphenyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]propanamide
N-cyclohexyl-3-{3-oxo-5-[({[4-(propan-2-yl)phenyl]carbamoyl}methyl)sulfanyl]-2H,3H-imidazo[1,2-c]quinazolin-2-yl}propanamide
N-cyclohexyl-3-[5-({[(4-methoxyphenyl)carbamoyl]methyl}sulfanyl)-3-oxo-2H,3H-imidazo[1,2-c]quinazolin-2-yl]propanamide
4-((2-(3-methoxyphenyl)-1,1-dioxido-3-oxo-2H-benzo[e][1,2,4]thiadiazin-4(3H)-yl)methyl)benzonitrile
2-(4-acetylphenyl)-4-ethyl-2H-1,2,4-benzothiadiazin-3(4H)-one 1,1-dioxide

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