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2-Allyloxy-4-chlorobenzoic acid is an organic compound with the chemical formula C10H9ClO3. It is a derivative of benzoic acid, featuring a chlorine atom at the 4-position, an allyl group at the 2-position, and a hydroxyl group attached to the allyl group. 2-allyloxy-4-chlorobenzoic acid is characterized by its molecular weight of 214.63 g/mol and a melting point of 76-77°C. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 2-Allyloxy-4-chlorobenzoic acid is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and antifungal agents. Its chemical properties include reactivity with nucleophiles due to the presence of the electron-withdrawing chlorine atom, which can facilitate substitution reactions.

5107-00-6

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5107-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5107-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5107-00:
(6*5)+(5*1)+(4*0)+(3*7)+(2*0)+(1*0)=56
56 % 10 = 6
So 5107-00-6 is a valid CAS Registry Number.

5107-00-6Relevant academic research and scientific papers

Oxidative cyclization of alkenoic acids promoted by AgOAc

Carrillo-Arcos, Ulises A.,Rojas-Ocampo, Jonathan,Porcel, Susana

supporting information, p. 479 - 483 (2016/01/09)

Alkenoic acids derived from salicylic acid and analogues undergo an unexpected oxidative cyclization process triggered by AgOAc leading to 4H-benzo[d][1,3]dioxin-4-ones. The process is affected by the substitution on the aryl and the allyl units.

General route for the preparation of diverse 17-membered macrocycles based on RCM and examination of the E/Z selectivity

Heckrodt, Thilo J.,Singh, Rajinder

, p. 2854 - 2865 (2012/07/16)

(Chemical Equation Presented) A convergent, general synthetic route to 17-membered macrocycles was developed to support biological evaluation and structure-activity relationship (SAR) studies during phenotypic screening for immunology targets. A series of amide coupling reactions led to a ring-closing metathesis (RCM) precursor that was cyclized using Grubbs' catalysts. It was found that the reaction formed the macrocyclic products in a 3:1 ratio of E/Z isomers. Moreover, it was shown that a number of similarly substituted RCM precursors undergo cyclization to produce the geometric E/Z isomers in roughly the same 3:1 ratio. The remarkable independence of the E/Z outcome from the substitution pattern of the RCM precursor makes this synthetic approach generally applicable. Separation of the E/Z isomers was achieved by preparative high-performance liquid chromatography and allowed biological profiling of the geometric isomers. Reactive groups in the macrocycle were utilized for late-stage modifications in the fashion of diversity-orientated synthesis (DOS), yielding analogs for SAR studies. Copyright Rigel Pharmaceuticals, Inc.

Regioselective silver-mediated Kondakov-Darzens olefin acylation

Barczak, Nicholas T.,Jarvo, Elizabeth R.

supporting information; experimental part, p. 12912 - 12916 (2011/12/04)

Enone construction: A silver-mediated olefin acylation reaction is described, in which five-, six-, and -seven-membered rings, tetrasubstituted olefins, bridged bicycles, spirocycles, and benzoxepinones are prepared. Highly selective intermolecular reactions are coupled to a Nazarov cyclization for the effective preparation of cyclopentenones, including the core of modhephene (see scheme). Copyright

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