Bis(4-methoxybenzoyl)methane

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Names

[ CAS No. ]:
18362-51-1

[ Name ]:
Bis(4-methoxybenzoyl)methane

[Synonym ]:
1,3-Propanedione, 1,3-bis(p-methoxyphenyl)-
1,3-bis(4-methoxyphenyl)propane-1,3-dione
1,3-Bis(4-methoxyphenyl)-1,3-propanedionato
1,3-Propanedione, 1,3-bis(4-methoxyphenyl)-
MFCD00025817
EINECS 242-233-2
1,3-Bis(p-methoxyphenyl)-1,3-propanedione
dianisoylmethane
Bis(4-methoxybenzoyl)methane
1,3-Di-(4-methoxyphenyl)-1,3-propanedione
1,3-BIS-(4-METHOXY-PHENYL)-PROPANE-1,3-DIONE
1,3-Bis(4-Methoxyphenyl)-1,3-propanedione

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
463.7±30.0 °C at 760 mmHg

[ Melting Point ]:
108-115ºC(lit.)

[ Molecular Formula ]:
C17H16O4

[ Molecular Weight ]:
284.306

[ Flash Point ]:
206.4±24.6 °C

[ Exact Mass ]:
284.104858

[ PSA ]:
52.60000

[ LogP ]:
3.19

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.560

MSDS

Safety Information

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

[ Hazard Codes ]:
Xn

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3.0

[ HS Code ]:
2914509090

Synthetic Route

Customs

[ HS Code ]: 2914509090

[ Summary ]:
HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Facile Route to Tetrasubstituted Pyrazoles Utilizing Ceric Ammonium Nitrate.

Synlett (9) , 1490-1494, (2009)

A convenient approach for the synthesis of tetrasubstituted pyrazoles is described. The method involves the treatment of 1,3-diketones and allyltrimethylsilane with CAN followed by cerium-catalyzed ad...

Thermostable and heat resistant aromatic polyethers based on heterocyclic bisphenols. Rusanov AL and Belomoina NM.

Polym. Sci., Ser. C 51(1) , 87-125, (2009)

β-Diketone reagents for the determination of borate in water. Lambert JL, et al.

Anal. Chem. 50(6) , 820-822, (1978)


More Articles


Related Compounds

  • 5-chloro-N-(1-cyclopropyl-5-oxopyrrolidin-3-yl)-2-methylbenzenesulfonamide
  • N-(1-cyclopropyl-5-oxopyrrolidin-3-yl)-4-(trifluoromethyl)benzenesulfonamide
  • methyl 3-(N-(1-cyclopropyl-5-oxopyrrolidin-3-yl)sulfamoyl)thiophene-2-carboxylate
  • N-(benzo[c][1,2,5]thiadiazol-4-yl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-2-carboxamide
  • 1-Cyclopropyl-2-(naphthalen-2-yloxy)ethanamine hydrochloride
  • N-(2-((4-methyl-4H-1,2,4-triazol-3-yl)thio)ethyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-2-carboxamide
  • N-benzyl-N-(propan-2-yl)-5H,6H,7H-pyrazolo[3,2-b][1,3]oxazine-2-carboxamide
  • N-ethyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-2-carboxamide
  • ethyl 2-(6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-2-carboxamido)acetate
  • N-(pyridin-2-ylmethyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-2-carboxamide
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