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2H-1-Benzopyran-2-one, 3-(2,3-dihydro-1-phenyl-2-thioxo-1H-imidazol-4-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88735-83-5

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88735-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88735-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,3 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88735-83:
(7*8)+(6*8)+(5*7)+(4*3)+(3*5)+(2*8)+(1*3)=185
185 % 10 = 5
So 88735-83-5 is a valid CAS Registry Number.

88735-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,3-dihydro-3-phenyl-2-thioxo-1H-imidazol-5-yl)-2H-chromen-2-one

1.2 Other means of identification

Product number -
Other names -

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:88735-83-5 SDS

88735-83-5Relevant academic research and scientific papers

Identification of novel molecular scaffolds for the design of MMP-13 inhibitors: A first round of lead optimization

La Pietra, Valeria,Marinelli, Luciana,Cosconati, Sandro,Di Leva, Francesco Saverio,Nuti, Elisa,Santamaria, Salvatore,Pugliesi, Isabella,Morelli, Matteo,Casalini, Francesca,Rossello, Armando,La Motta, Concettina,Taliani, Sabrina,Visse, Robert,Nagase, Hideaki,Da Settimo, Federico,Novellino, Ettore

experimental part, p. 143 - 152 (2012/03/09)

Osteoarthritis (OA) is the leading cause of joint pain and disability in middle-aged and elderly patients, and is characterized by progressive loss of articular cartilage. Among the various matrix metalloproteinases (MMPs), MMP-13 is specifically expresse

Efficient, stereoselective approach to the synthesis of 3-(1-Phenyl-2-(Z-styrylsulfonyl)-1H-imidazol-4-yl)-2H-chromen-2-ones

Guravaiah, Nalajam,Rao, Vedula Rajeswar

, p. 1167 - 1174 (2011/05/06)

Reaction of phenyl acetylene with 3-(1-aryl-2-mercapto-4-imidazolyl)-2H-1- benzopyran-2-ones (4) in the presence of sodium hydroxide in absolute ethanol led to the formation of 3-(1-phenyl-2-(Z-styrylthio)-1H-imidazol-4-yl)-2H- chromen-2-ones (6) in excel

Synthesis of 3-(1-aryl-2-mercapto-imidazolyl)-2H-1-benzopyran-2-one derivatives

Kumar, Ravi V.,Rao, V. Rajeswar

, p. 415 - 418 (2007/10/03)

Reaction of 3-(2-bromoacetyl) coumarins with various substituted aromatic primary amines resulted in the formation of 3-(2-anilino acetyl) coumarins 1 which on subsequent reaction with potassium thiocyanate furnishes corresponding 3-(1-aryl-2-mercapto-imi

α,β-UNSATURATED KETONES AND ANILIDES OF THE COUMARIN SERIES IN THE SYNTHESIS OF ISOXAZOLE, IMIDAZOLE, AND PYRAZOLE DERIVATIVES

Skripskaya, O. V.,Yagodinets, P. I.,Chernyuk, I. N.

, p. 1625 - 1627 (2007/10/03)

Coumarin-containing unsaturated ketones react with bromine to give dibromides, which form derivatives of isoxazoles and pyrazoles via reaction with hydroxylamine hydrochloride or phenylhydrazine.A method for preparing coumarin-containing imidazoles from the corresponding anilides was elaborated.

3-α-Bromacetyl-coumarines as Synthones for Heterocyclic Substituted Coumarines

Czerney, P.,Hartmann, H.

, p. 551 - 560 (2007/10/02)

3-α-Bromacetyl-coumarines 2 react easily and in high yields with thiourea and thioamide derivatives 3 and 5, resp., to 4-coumar-3'-yl-thiazoles 4 and 6, resp., as well as with N,N-disubstituted thioamides 11 and N,N,N',N'-tetraalkylthiourea 12 to 5-coumar-3'-yl-oxathioliumsalts 13 and 14, respectively.In a two-step reaction 2 can be transformed by reaction with aniline 17 to 4-coumar-3'-yl-imidazoles 21 and 5-coumar-3'-yl-oxazoliumsalts 22, resp., via aminoketone intermediates 18.

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