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1H-Indole, 3-(ethenylsulfonyl)-5-methoxy-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

847255-85-0

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847255-85-0 Usage

Derivative of indole

A heterocyclic organic compound

Methoxy group

A methoxy group (-OCH3) attached to the indole ring

Phenyl group

A phenyl group (-C6H5) attached to the indole ring

Potential for pharmaceutical research

May possess biological activity

Ethenylsulfonyl group

An ethenylsulfonyl group (-CH=CHSO2-) attached to the indole ring, adds to its potential reactivity and usefulness in chemical synthesis

Applications

Medicinal chemistry, organic synthesis, and as a building block for developing new compounds with various properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 847255-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,2,5 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 847255-85:
(8*8)+(7*4)+(6*7)+(5*2)+(4*5)+(3*5)+(2*8)+(1*5)=200
200 % 10 = 0
So 847255-85-0 is a valid CAS Registry Number.

847255-85-0Relevant academic research and scientific papers

Synthesis of anti-inflammatory, analgesic and COX-II inhibitory activities of indolylpyrazolines

Kumar, Ashok,Archana,Sharma, Shalabh,Malik, Nidhi,Sharma, Preeti,Kaushik, Kavita,Saxena, Kuldeep Kumar,Srivastava, Virendra Kishore,Verma,Sharma, Himansahu,Gupta,Gupta, Vipul,Agarwal

, p. 1532 - 1536 (2007/10/03)

Some 1-[N-phenylsulphonyl-3-(2′-substituted-3′-sulphonyl- 5′-methoxyindol-3′-yl)]-2-pyrazolines 7,8 and 1-[N-benzoyl-3- (2′-substituted-3′-sulphonyl-5′-methoxyindol-3yl)] -2-pyrazolines 5,6 have been synthesized by the reaction of 3-(2′- substituted-3′-sulphonyl-5′-methoxyindol-3′-yl)-2-pyrazolines 3,4 with benzenesulphonylehloride and benzoyl chloride respectively. The compounds of this series are screened for their anti-inflammatory, analgesic and COX-II inhibitory activities and compared with standard drugs, aspirin and indomethacin. The most active compound of this series is 1-[N-phenylsulphonyl-3- (2′-phenyl-3′-sulphonyl-5′-methoxyindol-3′-yl)] -2-pyrazoline 8.

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