Top quality factory supply 102-04-5 1,3-Diphenylacetone at low price

Q: What is the 1,3-Diphenylacetone?

1,3-Diphenylacetone is light yellow solid, while it's Molecular Formula is C15H14O. light yellow solid 1,3-Diphenylacetone is used in the aldol condensation reaction with benzil (a dicarbonyl) and base to create tetraphenylcyclopentadienone.

1,3-Diphenylacetone

CAS No.: 102-04-5
Purity: 99%

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1.What is the 1,3-Diphenylacetone ?

1,3-Diphenyl-2-propanone has a sweet, faint, fruity odor reminiscent of bitter almond

1,3-Diphenylacetone, also known as 1,3-diphenyl-2-propanone, is a light yellow solid with a sweet, faint, fruity odor reminiscent of bitter almond. It has a taste threshold value of 30 ppm, characterized by a bitter taste with floral, rose, and honey notes. In addition, its aroma threshold value at 10% in ethanol is described as sweet, powdery, and honey with floral rose nuances.

2.What is the CAS number for 1,3-Diphenylacetone ?

The CAS number of 1,3-Diphenylacetone is 102-04-5.

3.What are another words for 1,3-Diphenylacetone ?

Synonyms?for?1,3-Diphenylacetone 102-04-5:1,3-Diphenyl-2-propanone;2-Propanone,1,3-diphenyl-;1,3-Diphenylpropanone;Benzyl ketone;Dibenzyl ketone;NSC220312;NSC 407392;NSC 4577;a,a'-Diphenylacetone;

4.What is 1,3-Diphenylacetone (102-04-5) used for?

1,3-Diphenylacetone is used in the aldol condensation reaction with benzil (a dicarbonyl) and base to create tetraphenylcyclopentadienone.

InChI:InChI=1/C15H14O/c16-15(11-13-7-3-1-4-8-13)12-14-9-5-2-6-10-14/h1-10H,11-12H2

Relevant articles related to 1,3-Diphenylacetone:

Article	Source
Evidence for a 1,4-dioxy diradical as an intermediate in the thermal decomposition of 3,3-dibenzyl-1,2-dioxetane	Adam, Waldemar,Heil, Markus , p. 8807 - 8809 (1992)
Nickel-catalyzed cyanation of aryl halides and triflates using acetonitrile: Via C-CN bond cleavage assisted by 1,4-bis(trimethylsilyl)-2,3,5,6-tetramethyl-1,4-dihydropyrazine	Ueda, Yohei,Tsujimoto, Nagataka,Yurino, Taiga,Tsurugi, Hayato,Mashima, Kazushi , p. 994 - 999 (2019)
-	Selikson,Watt , p. 267 (1975)

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