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2,2-diphenyl-butyric acid-(2-diethylamino-ethyl ester) is a complex organic compound with the chemical formula C24H31NO2. It is a derivative of butyric acid, featuring a diphenyl group attached to the second carbon and a 2-diethylamino-ethyl ester group at the end. This ester is known for its potential applications in pharmaceuticals, particularly as a muscle relaxant. The compound's structure allows it to interact with certain receptors in the body, leading to its therapeutic effects. It is an ester derivative, which means it is formed by the reaction of an acid with an alcohol, in this case, butyric acid with 2-diethylamino-ethyl alcohol. The compound's properties, such as its solubility and stability, can be influenced by the presence of the diphenyl and diethylamino groups, making it a subject of interest in medicinal chemistry.

905-00-0

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905-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 905-00-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,0 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 905-00:
(5*9)+(4*0)+(3*5)+(2*0)+(1*0)=60
60 % 10 = 0
So 905-00-0 is a valid CAS Registry Number.

905-00-0Downstream Products

905-00-0Relevant academic research and scientific papers

Molecular Modification of Anticholinergics as Probes for Muscarinic Receptors. Amino Esters of α-Substituted Phenylacetic Acid and Related Analogues

Lu, Mattias C.,Wung, Walley E.,Shih, Lisa B.,Callejas, Soledad,Gearien, James E.,Thompson, Emmanuel B.

, p. 273 - 278 (2007/10/02)

Two series of compounds having the general structure of C6H5CRR'COOCH2CH2NEt2 were synthesized and examined for their antispasmodic activities.These compounds were selected as structural probes for exploring the nature of muscarinic cholinergic receptor binding sites that interact with atropine-like anticholinergics.These studies indicate a rather strict size limitation for the hydrophobic region of the receptor and suggest intramolecular hydrogen bonding as a possible means to explain the observed stereoselectivity.

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