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4-Thiazolidinone, 3-[5-[2-(4-chlorophenyl)ethenyl]-3-methyl-4-isoxazolyl]-2-(methylimino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

536710-14-2

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536710-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 536710-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 536710-14:
(8*5)+(7*3)+(6*6)+(5*7)+(4*1)+(3*0)+(2*1)+(1*4)=142
142 % 10 = 2
So 536710-14-2 is a valid CAS Registry Number.

536710-14-2Downstream Products

536710-14-2Relevant academic research and scientific papers

Synthesis of isoxazolylpyrazolo[3,4-d]thiazoles and isoxazolylthiazoles and their antibacterial and antifungal activity

Rajanarendar,Afzal,Karunakar

, p. 168 - 173 (2007/10/03)

Substituted methyl/phenyl-[3-(3-methyl-S-styryl-isoxazol-4-yl)-4-phenyl-3H- thiazol-2-ylidene]-amines 6, substituted-methyl/phenyl-[3-(3-methyl-S-styryl- isoxazol-4-yl)-thiazolidin-2-ylidene]-amines 7 and substituted 2-methyl/phenylimino-3-(3-methyl-5-styryl-isoxazol-4-yl)-thiazolidin-4-ones 3, have been synthesized by the reaction of substituted 1-methyl/phenyl-3-(3- methyl-5-styryl-isoxazol-4-yl)-thioureas 2 with phenacyl bromide, 1,2-dichloroethane and chloroacetic acid respectively. Condensation of 3 with aromatic aldehydes or interaction of 2 with ethyl chloroacetate and aromatic aldehydes in the presence of pyridine and piperidine in a single step, gives substituted-5-arylidene-2-methyl/phenylimino-3-(3-methyl-5-styryl-isoxazol-4-yl) -thiazolidin-4-ones 4, which are then cyclised to substituted [2-(2,4-dinitrophenyl)-6-(3-methyl-5-styryl-isoxazol-4yl)-3-aryl-2,3,3a, 6-tetrahydro-pyrazolo[3,4-d]thiazol-5-ylidene]-methyl/phenyl-amines 5 by reaction with 2,4-dinitrophenyl hydrazine in the presence of anhyd. sodium acetate. All the compounds have been evaluated for their antibacterial and antifungal activity.

Synthesis of isoxazolyl pyrimidine diones & isoxazolyl thiazolidinones

Rajanarendar,Afzal,Karunakar

, p. 353 - 357 (2007/10/03)

A series of 3-phenyl/methyl-1-(3-methyl-5-styryl/substituted styryl-4-isoxazolyl) -2,3-dihydro-2-thioxo-4,6(1H, 5H) pyrimidinediones 3 have been prepared from 1-phenyl/methyl-4-(3-methyl-5-styryl/substituted styryl-4-isoxazolyl)thioureas 2 by heating with malonic acid in acetyl chloride. Compounds 2 are obtained by interaction of 4-amino-3 -methyl-5-styryl/substituted styryl isoxazole 1 with phenyl and methyl isothiocyanates. The thioureas 2 when refluxed with chloroacetic acid and sodium acetate in absolute alcohol afford the corresponding 3-(3-methyl-5-styryl/substituted styryl-4-isoxazolyl)-2-phenyl/methyl imino-4-thiazolidinones 4. All the compounds have been evaluated for their biological activity.

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