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2-Pentenoic acid, 5-hydroxy-5-phenyl-, methyl ester is a complex organic compound with the chemical formula C12H14O3. It is a derivative of 2-pentenoic acid, featuring a hydroxyl group (-OH) and a phenyl group (C6H5) attached to the fifth carbon atom. The molecule is further characterized by the presence of a methyl ester group (-COOCH3), which is formed by the esterification of the carboxylic acid group with methanol. 2-Pentenoic acid, 5-hydroxy-5-phenyl-, methyl ester is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions, including esterification, and is used as an intermediate in the production of certain drugs and specialty chemicals.

4583-58-8

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4583-58-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4583-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4583-58:
(6*4)+(5*5)+(4*8)+(3*3)+(2*5)+(1*8)=108
108 % 10 = 8
So 4583-58-8 is a valid CAS Registry Number.

4583-58-8Downstream Products

4583-58-8Relevant academic research and scientific papers

Water-Compatible Synthesis of 2-Trifluoromethyl-1,3-Dioxanes

Becerra-Figueroa, Liliana,Tiniakos, Alexander F.,Prunet, Jo?lle,Gamba-Sánchez, Diego

supporting information, p. 6929 - 6932 (2018/11/25)

A water-compatible method for the diastereoselective synthesis of 2-trifluormethyl-1,3-dioxanes is described. The reaction proceeds under mild reaction conditions using simple inorganic bases; it has a very good substrate scope and can be performed with different Michael acceptors. Additionally, the reaction products can be further functionalized, showing an excellent perspective for future applications.

Synthesis of α-alkenyl-β-hydroxy adducts by α-addition of unprotected 4-bromocrotonic acid and amides with aldehydes and ketones by chromium(II)-mediated reactions

Wessjohann, Ludger A.,Wild, Harry,Ferreira, Leonildo A.,Schrekker, Henri S.

, p. 674 - 679 (2016/07/19)

The regioselective and diastereoselective chromium(II)-mediated reactions of 4-bromocrotonic acid or amides with aldehydes and ketones can proceed without the need to protect protic sites to generate the respective α-alkenyl-β-hydroxy adducts, i.e. formally the addition of the α-anion of a carboxylic acid or amide to an oxo-compound is featured.

α,β-unsaturated δ-lactones from copper-catalyzed asymmetric vinylogous mukaiyama reactions of aldehydes: Scope and mechanistic insights

Bazan-Tejeda, Belen,Bluet, Guillaume,Broustal, Garance,Campagne, Jean-Marc

, p. 8358 - 8366 (2007/10/03)

A direct regio-, diastereo-, and enantiocontrolled access to α,β-unsaturated δ-lactones is described, based on the reaction of a silyl dienolate and an aldehyde in the presence of 10% of Carreira's catalyst. The scope and limitations of this reaction, as well as mechanistic insights concerning the reactivity of an allyl copper species, are discussed.

A cobalt-phosphine complex as mediator in the formation of carbon-carbon bonds

Orsini,Pelizzoni,Pulici

, p. 1 - 3 (2007/10/02)

The tetrakis(trimethylphospine)cobalt(0) complex, [Co{P(CH3)3}4], in either stoichiometric or catalytic amounts, was shown to be an efficient mediator for a one-pot Reformatsky-type reaction between activated halogen derivatives (esters, amides, lactones) and carbonyl compounds (aldehydes, ketones) to produce a variety of alcohols.

REGIOSELECTIVE CONTROL OF ALLYL ANIONS WITH CADMIUM CHLORIDE: α vs. γ CONDENSATION WITH ALDEHYDES

Bo, Lei,Fallis, Alex G.

, p. 5193 - 5196 (2007/10/02)

A general method for directing the condensation of allyl anions such as 2 with aldehydes preferentially to the γ position of the unsaturated nucleophile is described.The procedure employs cadmium chloride to control the regioselectivity and will facilitat

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