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3-Penten-2-one, 4-(benzoyloxy)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36909-85-0

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36909-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36909-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36909-85:
(7*3)+(6*6)+(5*9)+(4*0)+(3*9)+(2*8)+(1*5)=150
150 % 10 = 0
So 36909-85-0 is a valid CAS Registry Number.

36909-85-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-oxopent-2-en-2-yl benzoate

1.2 Other means of identification

Product number -
Other names (Z)-1-methyl-3-oxo-1-enyl benzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36909-85-0 SDS

36909-85-0Downstream Products

36909-85-0Relevant academic research and scientific papers

Enzyme Promiscuity as a Remedy for the Common Problems with Knoevenagel Condensation

Koszelewski, Dominik,Ostaszewski, Ryszard

supporting information, p. 10156 - 10164 (2019/07/09)

A new protocol based on lipase-catalyzed tandem reaction toward α,β-enones/enoesters is presented. For the synthesis of the desired products the tandem process based on enzyme-catalyzed hydrolysis and Knoevenagel reaction starting from enol acetates and aldehyde is developed. The relevant impact of the reaction conditions including organic solvent, enzyme type, and temperature on the course of the reaction was revealed. It was shown that controllable release of the active methylene compound from the corresponding enol carboxylate ensured by enzymatic reaction diminishes significantly the formation of the unwanted co-products. Furthermore, this protocol was extended by including a second tandem chemoenzymatic transformation engaging various aldehyde precursors. After a careful optimization of the reaction conditions, the target products were obtained with yields up to 86 % and with excellent E/Z-selectivity.

Synthesis of isocoumarins via silver(I)-mediated annulation of enol esters

Panda, Niranjan,Mishra, Priyadarshini,Mattan, Irshad

, p. 1047 - 1056 (2016/02/19)

Silver-mediated annulation of 2-iodo enol esters leading to 4- and 3,4-substituted isocoumarins was accomplished selectively at room temperature. Coupling of 2-iodo benzoic acids with enolates that were produced in situ from the simple esters was also performed to produce isocoumarins under analogous reaction conditions. Owing to the mildness of the current protocol, 4-acyl 3-substituted isocoumarins were efficiently produced without any deacylation.

Reactions of nucleophilic carbenes with enols

Couture, Philippe,Pole, David L.,Warkentin, John

, p. 1565 - 1570 (2007/10/03)

The formal insertion of dimethoxycarbene (1a) into the acidic C-H bond of pentane-2,4-dione (9a), methyl acetoacetate (9b), 3-methylpentane-2,4-dione (9c) and 1,3-diphenylpropane-1,3-dione (9d) is reported as well as the insertion of 3-benzoyloxazolidin-2

Titanium-Induced Syntheses of Furans, Benzofurans and Indoles

Fuerstner, Alois,Jumbam, Denis N.

, p. 5991 - 6010 (2007/10/02)

Highly reactive titanium on graphite as the reagent of choice promotes intramolecular McMurry type reactions of acyloxy- and acylamido carbonyl compounds affording furans, benzofurans and indoles in good to excellent yields.A variety of reducible groups in the substrates is tolerated (e.g. -F, -Cl, -Br, -I, -CF3, -OMe, -CN, -thiophenyl, -COOR, -CONR2) and strained products such as 11h can be obtained, the X-ray analysis of which is reported.The experimental results indicate the possible formation of dianions from the aromatic aldehydes or ketones as reactive intermediates which attack the ester or amide functions in their proximity, rather than a radical path via ketyls.

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