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6296-54-4

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6296-54-4 Usage

General Description

ETHYL 2,4-DIOXO-4-PHENYLBUTANOATE is an organic compound with the chemical formula C12H12O4. It is a colorless liquid with a fruity odor, and it is commonly used as a flavoring agent in the food and beverage industry. It is also used in the production of perfumes and cosmetic products. ETHYL 2,4-DIOXO-4-PHENYLBUTANOATE is known for its sweet and fruity aroma, and it is often used to add a pleasant scent to various products. However, it is important to handle this chemical with care, as it can be harmful if ingested or inhaled in large quantities.

Check Digit Verification of cas no

The CAS Registry Mumber 6296-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6296-54:
(6*6)+(5*2)+(4*9)+(3*6)+(2*5)+(1*4)=114
114 % 10 = 4
So 6296-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O4/c1-2-16-12(15)11(14)8-10(13)9-6-4-3-5-7-9/h3-7H,2,8H2,1H3

6296-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,4-dioxo-4-phenylbutanoate

1.2 Other means of identification

Product number -
Other names ethyl-2,4-dioxo-4-phenylbutanonate

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:6296-54-4 SDS

6296-54-4Relevant articles and documents

Synthesis of pyrazine-2,3-dicarbonitriles via the one-pot three-component reaction of 4-benzoyl-5-phenylamino-2,3-dihydrothiophene-2,3-dione, diaminomaleonitrile, and functionalized alcohols in acetonitrile

Shahnaei, Roya,Kabirifard, Hassan,Fathololoomi, Parinaz

, p. 550 - 555 (2020)

An efficient one-pot three-component reaction of 4-benzoyl-5-phenylamino-2,3-dihydrothiophene-2,3-dione, diaminomaleonitrile, and alcohols with hetero-atom substituents or several hydroxyl groups in acetonitrile solvent under reflux led to the formation o

Reactions of 4-benzoyl-5-phenylamino-2,3-dihydrothiophene-2,3-dione and diaminomaleonitrile in the presence of alcohols as reactant and solvent

Moloudi, Maryam,Kabirifard, Hassan,Kabirifard, Raihaneh,Mahdikhani, Mona

, p. 347 - 356 (2017)

The one-pot synthesis of a novel class of 5-(2-alkoxy-2-phenyl-1-N-phenylthiocarbamoylethenyl)-6-oxo-1,6-dihydropyrazine-2,3-dicarbonitriles (2a–o) is achieved in moderate to good yields by the sequential reaction between 4-benzoyl-5-phenylamino-2,3-dihyd

Small-molecule vasopressin-2 receptor antagonist identified by a G-protein coupled receptor "pathway" screen

Yangthara, Buranee,Mills, Aaron,Chatsudthipong, Varanuj,Tradtrantip, Lukmanee,Verkman, Alan S.

, p. 86 - 94 (2007)

G-protein-coupled receptors (GPCRs) such as the vasopressin-2 receptor (V2R) are an important class of drug targets. We developed an efficient screen for GPCR-induced cAMP elevation using as read-out cAMP activation of cystic fibrosis transmemb

Design, synthesis, and biological activity evaluation of 2-(benzo[b]thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole derivatives as broad-spectrum antifungal agents

Zhao, Liyu,Sun, Yin,Yin, Wenbo,Tian, Linfeng,Sun, Nannan,Zheng, Yang,Zhang, Chu,Zhao, Shizhen,Su, Xin,Zhao, Dongmei,Cheng, Maosheng

, (2021/11/22)

To discover antifungal compounds with broad-spectrum and stable metabolism, a series of 2-(benzo[b]thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole derivatives was designed and synthesized. Compounds A30-A34 exhibited excellent broad-spectrum antifungal activity against Candida albicans with MIC values in the range of 0.03–0.5 μg/mL, and against Cryptococcus neoformans and Aspergillus fumigatus with MIC values in the range of 0.25–2 μg/mL. In addition, compounds A31 and A33 showed high metabolic stability in human liver microsomes in vitro, with the half-life of 80.5 min and 69.4 min, respectively. Moreover, compounds A31 and A33 showed weak or almost no inhibitory effect on the CYP3A4 and CYP2D6. The pharmacokinetic evaluation in SD rats showed that compound A31 had suitable pharmacokinetic properties and was worthy of further study.

RETRACTED ARTICLE: IspH inhibitors kill Gram-negative bacteria and mobilize immune clearance

Singh, Kumar Sachin,Sharma, Rishabh,Reddy, Poli Adi Narayana,Vonteddu, Prashanthi,Good, Madeline,Sundarrajan, Anjana,Choi, Hyeree,Muthumani, Kar,Kossenkov, Andrew,Goldman, Aaron R.,Tang, Hsin-Yao,Totrov, Maxim,Cassel, Joel,Murphy, Maureen E.,Somasundaram, Rajasekharan,Herlyn, Meenhard,Salvino, Joseph M.,Dotiwala, Farokh

, p. 597 - 602 (2020/12/25)

Isoprenoids are vital for all organisms, in which they maintain membrane stability and support core functions such as respiration1. IspH, an enzyme in the methyl erythritol phosphate pathway of isoprenoid synthesis, is essential for Gram-negati

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