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Spiro[3H-indole-3,2'-thiazolidine]-2,4'(1H)-dione, 3'-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79962-57-5

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79962-57-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79962-57-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,6 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79962-57:
(7*7)+(6*9)+(5*9)+(4*6)+(3*2)+(2*5)+(1*7)=195
195 % 10 = 5
So 79962-57-5 is a valid CAS Registry Number.

79962-57-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)spiro[1,3-thiazolidine-2,3'-1H-indole]-2',4-dione

1.2 Other means of identification

Product number -
Other names HMS623N05

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:79962-57-5 SDS

79962-57-5Downstream Products

79962-57-5Relevant academic research and scientific papers

The influence of the polymerization approach on the catalytic performance of novel porous poly (ionic liquid)s for green synthesis of pharmaceutical spiro-4-thiazolidinones

Elyasi, Zahra,Monfared, Mohammad Reza Zand,Najafi, Gholam Reza,Safaei Ghomi, Javad

, p. 44159 - 44170 (2020/12/25)

Although poly (ionic liquids) (PILs) have attracted great research interest owing to their various applications, the performance of nanoporous PILs has been rarely developed in the catalysis field. To this end, a micro-mesoporous PIL with acid-base bifunc

Synthesis, partition coefficients and antibacterial activity of 3′-phenyl (substituted)-6′-aryl-2′(1H)-cis-3′,3′ a -dihydrospiro[3-H-indole-3,5′-pyrazolo (3′,4′-d)-thiazolo-2- (1H)-ones]

Sahu, Susant K.,Banerjee, Mrityunja,Mishra, Sagar K.,Mohanta, Raj K.,Panda, Prasanna K.,Misro, Prafulla K.

, p. 121 - 126 (2008/09/17)

Condensation of isatin with primary aryl amines gave a series of Schiff bases (1) which on reaction with thioglycolic acid in 1,4-dioxane afforded the formation of the corresponding 4- thiazolidinones (2). Compound 2 on condensation with substituted benza

Synthesis, partition coefficient and antibacterial activity of 3′-aryl-6′-phenyl(substituted)-cis-5′a,6′- dihydrospiro[3H-indole-3,4′-thiozolo(5′,1′-c)-isoxazolo-2-(1H) -ones]

Sahu,Mishra,Banerjee,Panda,Misro

, p. 725 - 727 (2007/10/03)

Condensation of isatin with primary aryl amines gave a series of Schiff bases (1) which on reaction with thioglycolic acid in 1,4-dloxane afforded the corresponding thiazolidones (2). Compound 2 on condensation with substituted benzaldehydes in anhydrous

SYNTHESIS OF SOME NEW SPIROHETEROCYCLES RELATED TO SPIROOXATHIALANE>-2,5'-DIONE

Al-Thebeiti, Marzoog S.,El-Zohry. Maher F.

, p. 251 - 256 (2007/10/02)

The reaction of indole-2,3-dione (1a) and/or 1-methylindole-2,3-dione (1b) with mercaptoacetic acid in the presence of 4-toluenesulfonic acid as a catalyst afforded spirooxathialane>-2,5'-diones (2a, b).Compounds 2a and/or 2 b were reacted with the appropriate aliphatic and/or aromatic primary amines to give compounds 3a-j.The reaction of 2a, b with hydrazine hydrate, phenylhydrazine and p-nitrophenylhydrazine yielded spiroderivatives 4a-c.Friedel-Crafts reactions of 2a and 2b with arenes in the presence of aluminium chloride catalyst afforded spiroindoline isothiochroman derivatives 5a-h.Key words: Spiroindoline derivatives; spiroheterocycles; NMR.

A CONVENIENT SYNTHESIS AND REACTION OF SPIRO -2,4'(1h)-DIONES

Joshi, Krishna C.,Patni, R.,Chand, Pooran

, p. 1555 - 1559 (2007/10/02)

Spiro-2,4'(1H)-diones have been obtained by the condensation of indole-2,3-dione, aromatic amine and mercaptoacetic acid without isolating the intermediates i.e., isatin-3-anils.The spiro compounds have further been subjected

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