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2-(1-(Thiophen-2-ylMethyl)cyclohexyl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78645-45-1

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78645-45-1 Usage

General Description

2-(1-(Thiophen-2-ylMethyl)cyclohexyl)acetic acid is a chemical compound with the molecular formula C16H22O2. It is a derivative of cyclohexylacetic acid and contains a thiophene ring. The compound is commonly used in pharmaceutical research and development as a potential drug candidate due to its effects on biological systems. It is known to possess anti-inflammatory and analgesic properties, making it a promising candidate for the treatment of various inflammatory conditions and pain disorders. Additionally, 2-(1-(Thiophen-2-ylMethyl)cyclohexyl)acetic acid has shown potential in the treatment of neurological disorders and has been studied for its potential as a therapeutic agent for conditions such as epilepsy and neurodegenerative diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 78645-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78645-45:
(7*7)+(6*8)+(5*6)+(4*4)+(3*5)+(2*4)+(1*5)=171
171 % 10 = 1
So 78645-45-1 is a valid CAS Registry Number.

78645-45-1Downstream Products

78645-45-1Relevant academic research and scientific papers

Synthesis of thienospiran derivatives and studies of regioselectivity in Friedel-Crafts acylation reaction

Sen,Saha, Uttam Kumar,Das, Tulika

, p. 648 - 656 (2007/10/03)

Syntheses of several spiro[benzo[b]thiophen-6(5H),1'-cycloalkan]-4(7H)- ones (Type A) and spiro[benzo[b]thiophen-5,1'-cycloalkan]-4(5H)-ones (Type B) and their 2-alkyl derivatives are described. The regioselectivity in the Friedel-Crafts acylation of thiophenes with anhydride of various unsymmetrically substituted succinic acid having substituent(s) at the same carbon atom in two different solvents namely dichloromethane and nitrobenzene is studied. A plausible explanation of such regioselective acylation of thiophenes has been incorporated.

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