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2H-Pyran-3-carbonitrile, 6-(4-fluorophenyl)-4-(methylthio)-2-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153391-26-5

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153391-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153391-26-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,9 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 153391-26:
(8*1)+(7*5)+(6*3)+(5*3)+(4*9)+(3*1)+(2*2)+(1*6)=125
125 % 10 = 5
So 153391-26-5 is a valid CAS Registry Number.

153391-26-5SDS

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 6-(4-fluorophenyl)-4-methylsulfanyl-2-oxopyran-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-(4-fluorophenyl)-4-methylsulfanyl-2H-pyran-2-one-3-carbonitrile

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:153391-26-5 SDS

153391-26-5Relevant academic research and scientific papers

Base-mediated alternate route for multi-functionalized allylbenzenes using ring transformation strategy

Shetgaonkar, Samata E.,Singh, Fateh V.

, p. 2511 - 2521 (2020/07/09)

A simple yet innovative approach for the construction of multi-substituted allylbenzenes 14, 16 and 18 with ‘donor-acceptor’ functionalities has been delineated through base-mediated ring transformation of 6-aryl-2H-pyran-2-ones 13, 15 and 17 respectively

Transition metal-free synthesis of sterically hindered allylarenes from 5-hexene-2-one

Althagafi, Ismail,Elagamy, Amr,Nemaysh, Vishal,Pratap, Ramendra,Rai, Reeta,Shah, Chandan,Shaw, Ranjay,Singh, Harpreet

supporting information, p. 6276 - 6286 (2020/09/07)

A simple, efficient and transition metal-free strategy was established for the synthesis of highly functionalized, sterically hindered allylarenes (6, 7 & 8) by base-mediated ring transformation of 2-oxo-6-aryl-4-(methylthio/sec-amino)-2H-pyran-3-carbonit

Synthesis of Solution-Processable Donor-Acceptor Pyranone Dyads for White Organic Light-Emitting Devices

Sharma, Chandra P.,Gupta, Neeraj M.,Singh, Jagriti,Yadav, Rohit Ashok Kumar,Dubey, Deepak Kumar,Rawat, Kundan S.,Jha, Ajay K.,Jou, Jwo-Huei,Goel, Atul

, p. 7674 - 7684 (2019/06/27)

A series of donor-acceptor pyranones (3a-m, 4a-h) were synthesized using α-oxo-ketene-S,S-acetal as the synthon for their application as emissive materials for energy-saving organic light-emitting devices (OLEDs). Among them, five pyranones 3f, 3g, 3h, 3m

Base-promoted regioselective synthesis of 1,2,3,4-terahydroquinolines and quinolines from N-boc-3-piperidone

Shally,Althagafi, Ismail,Singhal, Divya,Panwar, Rahul,Shaw, Ranjay,Elagamy, Amr,Pratap, Ramendra

, (2019/11/11)

An efficient synthesis of 1,2,3,4-tetrahydroquinolines with donor and acceptor group has been delineated by base mediated ring transformation of 6-aryl-4-substituted-2H-pyran-2-one-3-carbonitriles by N-boc-3-piperidone followed by consecutive deprotection

Chemoselective synthesis of m-teraryls through ring transformation of 2 H-pyran-2-ones by 2-(1-arylethylidene)-malononitriles

Panwar, Rahul,Shally,Shaw, Ranjay,Elagamy, Amr,Pratap, Ramendra

, p. 8994 - 9002 (2018/12/10)

We have developed a simple, efficient and chemoselective approach for the synthesis of m-teraryls by the reaction of 6-aryl-2-oxo-4-(sec.amino)-2H-pyran-3-carbonitriles and 2-(1-arylethylidene)malononitriles under basic conditions. We used 6-aryl-2-oxo-4-

Photophysical and electrochemical studies of highly fluorescent pyrazole and imidazole containing heterocycles

Maurya, Hardesh K.,Kumar, Ch. Pavan,Chandrasekharam,Gupta, Atul

, p. 686 - 696 (2016/09/28)

Highly congested pyrazole and imidazole ring containing heterocycles were studied for their photophysical and electrochemical properties. TDDFT calculations of the molecules were carried out using B3LYP/G(d,p) level theory in DMF medium and the results we

Microwave directed metal-free regiodivergent synthesis of 1,2-teraryls and study of supramolecular interactions

Singh, Surjeet,Shally,Shaw, Ranjay,Yadav, Reena,Kumar, Abhinav,Pratap, Ramendra

, p. 14768 - 14777 (2016/02/19)

A microwave directed, simple and efficient synthesis of 3′-amino-5′-(sec.amino)-[1,1′:2′,1′′-teraryl]-4′-carbonitriles has been delineated through ring transformation reaction of 6-aryl-2-oxo-4-sec.amino-2H-pyran-3-carbonitriles by benzyl cyanide under ba

Base mediated regioselective synthesis of highly functionalized conjugated enones

Singh, Surjeet,Panwar, Rahul,Althagafi, Ismail,Sharma, Vashundhara,Chaudhary, Sandeep,Pratap, Ramendra

, p. 5203 - 5208 (2015/08/19)

A simple, regioselective, convenient, and base mediated synthesis of (2E,4E)-5-aryl-6-oxo-6-phenyl-3-sec.amino-hexa-2,4-dienenitriles has been achieved by the reaction of 6-aryl-4-sec.amino-2-oxo-2H-pyran-3-carbonitriles and benzyl cyanide. This reaction

A carbanion induced synthesis of highly congested pyrazole and imidazole containing heterocycles

Maurya, Hardesh K.,Gupta, Atul

, p. 1715 - 1719 (2014/03/21)

An efficient approach to the synthesis of highly congested di, penta and hexacyclic pyrazoles as well as imidazole fragment containing novel heterocyclic molecule has been developed through a carbanion induced transformation of suitably functionalized 2H-

Synthesis and glycosidase inhibitory activity of novel (2-phenyl-4H- benzopyrimedo[2,1-b]-thiazol-4-yliden)acetonitrile derivatives

Patil, Vijay S.,Nandre, Kamalakar P.,Ghosh, Sougata,Rao, Vaidya Jayathirtha,Chopade, Balu A.,Bhosale, Sheshanath V.,Bhosale, Sidhanath V.

, p. 7011 - 7014 (2013/01/15)

A series of (2-phenyl-4H-benzopyrimodo[2,1-b][1,3]thiazol-4-yliden-4- yliden)acetonitrile derivatives have been prepared by ring transformation reaction of 4-(methylthio)-2-oxo-6-aryl-2H-pyrane-3-carbonitriles. The yield of ring transformation product is

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