BENZYL ACETOACETATE

Q: What is the BENZYL ACETOACETATE?

BENZYL ACETOACETATE is clear colorless to yellow liquid, while it's Molecular Formula is C11H12O3. clear colorless to yellow liquid Benzyl acetoacetate (AAbenzyl) is chemical intermediate used for the syntheses of different organic chemicals Product Data Sheet

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1.What is the BENZYL ACETOACETATE ?

Benzyl acetoacetate has a sweet, floral, fresh, balsamic, fruity odor similar to that of ethyl acetate.

Benzyl acetoacetate, also known as AAbenzyl, is a chemical intermediate derived from organic chemicals and is known for its sweet, floral, fresh, balsamic, and fruity odor, which is similar to that of ethyl acetate. It undergoes asymmetric bioreduction to form benzyl (S)-(+)-3-hydroxybutyrate in the presence of Candida schatavii strain MY 1831. Benzyl acetoacetate has been reported to be found in litchi (Litchi sinensis Sonn.).

2.What is the CAS number for BENZYL ACETOACETATE ?

The CAS number of BENZYL ACETOACETATE is 5396-89-4.

3.What are another words for BENZYL ACETOACETATE ?

Synonyms?for?BENZYL ACETOACETATE 5396-89-4:Acetoaceticacid, benzyl ester (6CI,8CI);3-Oxobutanoic acid benzyl ester;3-Oxobutanoicacid phenylmethyl ester;Benzyl 3-oxobutanoate;Benzyl acetoacetate;Benzylacetylacetate;NSC 4391;Phenylmethyl 3-oxobutanoate;

4.What is BENZYL ACETOACETATE (5396-89-4) used for?

Benzyl acetoacetate (AAbenzyl) is chemical intermediate used for the syntheses of different organic chemicals Product Data Sheet

InChI:InChI=1/C11H12O3/c1-9(12)7-11(13)14-8-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3

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A simple and efficient preparation of propargylic β-keto esters through transesterification	Mottet,Hamelin,Garavel,Depres,Greene , p. 1380 - 1382 (1999)
Revisiting ageless antiques; synthesis, biological evaluation, docking simulation and mechanistic insights of 1,4-Dihydropyridines as anticancer agents	Sidhom, Peter A.,El-Bastawissy, Eman,Salama, Abeer A.,El-Moselhy, Tarek F. supporting information, (2021/06/21)
Design, synthesis, and molecular docking study of new monastrol analogues as kinesin spindle protein inhibitors	El-Hamamsy, Mervat H.,Sharafeldin, Nabaweya A.,El-Moselhy, Tarek F.,Tawfik, Haytham O. , (2020/06/03)

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