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3-Phenyl-4-acetyl-1,2,3-oxadiazole-3-ium-5-olate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13973-33-6

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13973-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13973-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,7 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13973-33:
(7*1)+(6*3)+(5*9)+(4*7)+(3*3)+(2*3)+(1*3)=116
116 % 10 = 6
So 13973-33-6 is a valid CAS Registry Number.

13973-33-6SDS

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 4-acetyl-3-phenyloxadiazol-3-ium-5-olate

1.2 Other means of identification

Product number -
Other names 4-Acetyl-3-phenyl-1,2,3-oxadiazol-3-ium-5-olate

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:13973-33-6 SDS

13973-33-6Relevant academic research and scientific papers

Metal triflate-catalyzed friedel-crafts acetylation of 3-phenylsydnone

Balaguer, Amanda,Selhorst, Ryan,Turnbull, Kenneth

, p. 1626 - 1632 (2013)

Friedel-Crafts acetylation at the 4-position of 3-phenylsydnone (1) was achieved via thermal heating overnight in moderate to good yields by employing various metal triflate catalysts (5-20 mol%), lithium perchlorate (0-20 mol%), and acetic anhydride (4 e

Synthesis of aminopyrazoles from sydnones and ynamides

Wezeman,Comas-Barceló,Nieger,Harrity,Br?se

supporting information, p. 1575 - 1579 (2017/02/23)

Aminopyrazoles are prepared from readily accessible sydnones and sulfonyl ynamides using either a copper-mediated sydnone alkyne cycloaddition (CuSAC) or in situ generated strained cyclic ynamides.

Pyridine-catalyzed synthesis of quinoxalines as anticancer and anti-tubercular agents

Kamble, Atulkumar A.,Kamble, Ravindra R.,Kumbar, Mahadev N.,Tegginamath, Gireesh

, p. 1163 - 1174 (2016/07/06)

Quinoxaline derivatized with coumarin viz., 3a–f and with sydnones viz., 7a–0 were synthesized using pyridine as catalyst. Among the coumarin derivatives, 3a and 3b have been screened for anticancer activity against 60 human cancer cell lines at NIH (USA)

1,3-Dipolar cycloaddition between acetylenic dipolarophiles and sydnone-N-ylides as bis(1,3-dipoles)

Albota, Florin,Dr?ghici, Constantin,Caira, Mino R.,Dumitrascu, Florea

, p. 9095 - 9100 (2015/11/09)

1,3-Dipolar cycloaddition reaction of sydnone-N-ylides, as model bis(1,3-dipoles), with acetylenic dipolarophiles in 1,2-epoxybutane under reflux gave exclusively pyrroloazines containing a sydnone moiety that resulted by preferred reaction of the N-ylide

Bismuth triflate-catalyzed friedel-crafts acylations of sydnones

Mahoney, Jennifer,Turnbull, Kenneth,Cubberley, Mark

, p. 3220 - 3229 (2012/11/07)

Friedel-Crafts acylations of various 3-arylsydnones at the C4 position have been achieved in good yields using 4 equivalents of an alkyl anhydride and 25mol% each of bismuth triflate and lithium perchlorate in anhydrous acetonitrile at 95C. Acylations app

Synthesis of 2 H-indazoles by the [3 + 2] dipolar cycloaddition of sydnones with arynes

Fang, Yuesi,Wu, Chunrui,Larock, Richard C.,Shi, Feng

, p. 8840 - 8851 (2012/01/02)

A rapid and efficient synthesis of 2H-indazoles has been developed using a [3 + 2] dipolar cycloaddition of sydnones and arynes. A series of 2H-indazoles have been prepared in good to excellent yields using this protocol, and subsequent Pd-catalyzed coupl

N-Bromosuccinimide (NBS) as Promoter for Acylation of Sydnones in the Presence of Acetic Anhydride under Neutral Conditions

Ghasemnejad-Bosra, Hassan,Haghdadi, Mina,Gholampour-Azizi, Issa

, p. 391 - 395 (2008/09/20)

Various 4 - acetyl sydnones (2) can be prepared by reaction of the corresponding 3-aryl sydnones (1) with acetic anhydride at ~110 °C promoted by N-Bromosuccinimide (NBS) as an effective reagent for acylation of sydnones under neutral conditions in satisf

Synthesis and biological study of some novel 4-[5-(4,6-disubstituted-2- thiomethylpyrimidyl)-4'-amino-1,2,4- triazol-3'-yl] thioacetyl-3-arylsydnones

Kalluraya, Balakrishna,Lingappa,Nooji, Satheesh Rai

, p. 1393 - 1401 (2008/02/07)

A series of 4-[5-(4,6-disubstituted-2-thiomethyl pyrimidyl)-4'-amino-1,2-4- triazol-3'-yl]thioacetyl-3-arylsydnones 7a-i were synthesized by the reaction of 5-(4,6-disubstituted-2-thiomethylpyrimidyl)-4-amino-3-mercapto-1,2-4-triazoles 3 with 3-aryl-4-bromoacetyl sydnones 6 in an ethanol medium. The newly synthesized compounds 7a-i were screened for their antibacterial activity against E. coli and Serratia marcesens and for antibacterial activity against Aspergillus niger and Pencillium. Most of the tested compounds showed significant antifungal activity particularly against Pencillium at 10-g/mL concentration comparable with that of the standard drug Flukanazole.

1,3-Dibromo-5,5-dimethylhydantoin (DBH) as an efficient promoter for acetylation of 3-arylsydnones in the presence of acetic anhydride under neutral conditions

Azarifar, Davood,Bosra, Hassan Ghasemnejad,Tajbaksh, Mahmood

, p. 467 - 469 (2008/03/29)

(Chemical Equation Presented) 1,3-Dibromo-5,5-dimethylhydantoin (DBH) has been found to efficiently promote the conversion of various 3-arylsydnones to their 4-acetyl congeners in the presence of acetic anhydride under neutral conditions in satisfactory y

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