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Phenol, 4-(dimethylamino)-, acetate (ester), also known as 4-(dimethylamino)phenol acetate or acetaminophen, is an organic compound with the chemical formula C8H11NO2. It is a colorless, crystalline solid that is soluble in water, ethanol, and chloroform. Phenol, 4-(dimethylamino)-, acetate (ester) is widely used as an analgesic and antipyretic drug, commonly known as paracetamol or acetaminophen. It is effective in relieving mild to moderate pain and reducing fever. The acetate ester form of the compound is less polar than the parent phenol, which can affect its solubility and absorption in the body. It is important to note that while it is a widely used medication, it can have serious side effects if not used properly, including liver damage in cases of overdose.

2436-77-3

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2436-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2436-77-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2436-77:
(6*2)+(5*4)+(4*3)+(3*6)+(2*7)+(1*7)=83
83 % 10 = 3
So 2436-77-3 is a valid CAS Registry Number.

2436-77-3Relevant academic research and scientific papers

Copper-Catalyzed Acetylation of Electron-Rich Phenols and Anilines

Zhang, Jieyu,Ke, Qiumin,Tian, Feitao,Jiang, Bei,Ji, Chang-An,Zhang, Lingling,Yu, Jian,Huang, Dayun,Yan, Guobing

supporting information, p. 726 - 730 (2019/03/26)

An approach has been developed for the copper-catalyzed acetylation of phenols and anilines with potassium thioacetate as an acetylating reagent. Although only electron-rich phenols and anilines are compatible with this protocol, the reaction can provide moderate to high yields under mild conditions. Compared with other acetylating reagents, the current reagent has certain advantages, such as its low cost, easy availability, stability, insensitivity to water or air, and ease of storage.

Transformation of N, N-Dimethylaniline N-Oxides into Diverse Tetrahydroquinoline Scaffolds via Formal Povarov Reactions

Bush, Timothy S.,Yap, Glenn P. A.,Chain, William J.

supporting information, p. 5406 - 5409 (2018/09/13)

A one-pot protocol for the assembly of diversely functionalized tetrahydro-, hexahydrofuro-, hexahydropyrano-, and tetrahydrobenzofuroquinolines from N,N-dimethylaniline N-oxides and various electron-rich olefins in a tandem Polonovski-Povarov sequence is reported. Following activation of the N-O bond with Boc2O, an exocyclic iminium ion is unveiled upon exposure to tin(IV) chloride. A formal inverse-electron-demand aza-Diels-Alder cyclization generates the tetrahydroquinoline core of 29 examples in up to 92% yield.

NON-SOLVENT SYSTEM ADHESIVE COMPOSITION FOR DENTISTRY

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Paragraph 0100, (2017/07/18)

PROBLEM TO BE SOLVED: To provide a non-solvent system adhesive composition for dentistry which exhibits excellent adhesiveness to any of dental enamel and dentin, and substantially contains neither water nor an organic solvent. SOLUTION: The invention provides a non-solvent system adhesive composition for dentistry containing neither water nor an organic solvent, wherein (A) a polymerizable monomer component,(B) aromatic amine having an electron withdrawing group, and(C) a polymerization initiator are contained; and the polymerizable monomer component (A) contains a phosphoric acid monomer (a1) having a phosphate acidic group (>P(=O)OH) and a sulfonic acid monomer (a2) having a sulfonic acid group at the following mass ratio; (a1):(a2)=98:2-67:33, and simultaneously contains the sulfonic acid monomer (a2) and the aromatic amine (B) at a ratio so that the molar ratio of an aromatic amino group and a sulfonic acid group (the aromatic amino group/sulfonic acid group) becomes 0.8 or more. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Oxyaniliniums as acetylcholinesterase inhibitors for the reversal of neuromuscular block

Grove, Simon J.A.,Kaur, Jasmit,Muir, Alan W.,Pow, Eleanor,Tarver, Gary J.,Zhang, Ming-Qiang

, p. 193 - 196 (2007/10/03)

A series of oxyanilinium-based AChE inhibitors have been synthesised and tested for the reversal of vecuronium-induced neuromuscular block. Several compounds, for example 2-hydroxy- and 2-methoxy-N,N-dimethyl-N-allylanilinium bromide (3 and 6) showed comparable reversal potencies to edrophonium and clean in vivo cardiovascular profiles.

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