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Benzenepropanoic acid, 4-(dimethylamino)-, ethyl ester, also known as procaine, is an organic compound with the chemical formula C13H20N2O2. It is a derivative of benzoic acid, featuring a dimethylamino group at the 4-position and an ethyl ester group at the carboxyl group. Procaine is a widely used local anesthetic, primarily in dentistry and ophthalmology, due to its ability to block nerve conduction by inhibiting the sodium channels in nerve cells. It is also known for its rapid onset and short duration of action. The compound is synthesized by esterifying 4-(dimethylamino)benzoic acid with ethanol, and its molecular structure contributes to its stability and effectiveness as an anesthetic agent.

7116-46-3

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7116-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7116-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7116-46:
(6*7)+(5*1)+(4*1)+(3*6)+(2*4)+(1*6)=83
83 % 10 = 3
So 7116-46-3 is a valid CAS Registry Number.

7116-46-3Downstream Products

7116-46-3Relevant academic research and scientific papers

CoBr2(Bpy): An efficient catalyst for the direct conjugate addition of aryl halides or triflates onto activated olefins

Amatore, Muriel,Gosmini, Corinne,Perichon, Jacques

, p. 6130 - 6134 (2007/10/03)

An efficient cobalt-catalyzed method devoted to the direct conjugate addition of functionalized aryl compounds onto Michael acceptors is described. The CoBr2(2,2′-bipyridine) complex appears to be an extremely suitable catalyst for the activation of a variety of aromatic reagents ranging from halides to triflates functionalized by reactive groups. This procedure allows for the synthesis of compounds resulting from 1,4-addition in good to excellent yields. The versatility of this original process represents a simple alternative to most known methods using organometallic reagents.

Electrochemical vinylation of aryl and vinyl halides with acrylate esters catalyzed by cobalt bromide

Gomes, Paulo,Gosmini, Corinne,Nédélec, Jean-Yves,Périchon, Jacques

, p. 5901 - 5903 (2007/10/03)

A consumable anode process permits the electrochemical Heck reaction between aromatic or vinylic halides and acrylate esters using cobalt bromide as catalyst associated with bipyridine as ligand in a mixture of acetonitrile/triethylamine/pyridine as solvent.

PHENYL ALKYLAMINOPYRIMIDONES

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, (2008/06/13)

The compounds are phenyl alkylaminopyrimidones which are histamine H. sub.2-antagonists. A specific compound of the present invention is 2-[2-[3-(dimethylaminomethyl)benzylthio]ethylamino]-5-(6-methyl-3-pyridylme thyl)-4-pyrimidone.

GUANIDINOTHIAZOLYL DERIVATIVES

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, (2008/06/13)

The compounds are guanidinothiazolyl derivatives which are histamine H. sub.2-antagonists. A specific compound of the present invention is 2-2-(2-guanidino-4-thiazolylmethylthio)ethylamino!-5-(6-methyl-3-pyridylmethy l)-4-pyrimidone.

ISOUREAS AND ISOTHIOUREAS

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, (2008/06/13)

The compounds are isoureas and isothioureas which have an O-or S-alkylpyrimidone substituent and which are histamine H 2-antagonists and antiinflammatory agents. A specific compound of this invention is 2-[5-(O-isoureido)pentylamino]-5-(6-methyl-3-pyridylmethyl)-4-pyrimidone.

Pyrimidine compounds

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, (2008/06/13)

The compounds are substituted pyrimidine compounds which are histamine H2 -antagonists. A specific compound of the present invention is 2-[2-(5-dimethylaminomethyl)-2-furylmethylthio)ethylamino]-5-(3-pyridylmethyl)-4-pyrimidone.

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