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D-erythro-2-amino-3-cyclohexyl-3-hydroxypropionic acid, also known as D-EACP, is a synthetic amino acid derivative with a unique chemical structure. It features a cyclohexane ring, which is a six-carbon ring structure, and a hydroxypropionic acid group, indicating the presence of a hydroxyl (-OH) and a carboxyl (-COOH) group. D-erythro-2-amino-3-cyclohexyl-3-hydroxypropionic acid is a chiral molecule, meaning it has a non-superimposable mirror image, and the "D" prefix signifies the dextrorotatory form, which is the right-handed configuration in its spatial arrangement. D-EACP has potential applications in various fields, including pharmaceuticals and materials science, due to its specific chemical properties and reactivity.

5962-92-5

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5962-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5962-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5962-92:
(6*5)+(5*9)+(4*6)+(3*2)+(2*9)+(1*2)=125
125 % 10 = 5
So 5962-92-5 is a valid CAS Registry Number.

5962-92-5Downstream Products

5962-92-5Relevant academic research and scientific papers

Pd-catalyzed intramolecular aminohydroxylation of alkenes with hydrogen peroxide as oxidant and water as nucleophile

Zhu, Haitao,Chen, Pinhong,Liu, Guosheng

supporting information, p. 1766 - 1769 (2014/03/21)

A palladium-catalyzed intramolecular aminohydroxylation of alkenes was developed, in which H2O2 was applied as the sole oxidant. A variety of related alkyl alcohols could be successfully obtained with good yields and excellent diastereoselectivities, which directly derived from oxidation cleavage of alkyl C-Pd bond by H2O2. Facile transformation of these products provided a powerful tool toward the synthesis of 2-amino-1,3-diols and 3-ol amino acids. Preliminary mechanistic studies revealed that major nucleophilic attack of water (SN2 type) at high-valent Pd center contributes to the final C-O(H) bond formation.

Direct-type aldol reactions of fluorenylidene-protected/activated glycine esters with aldehydes for the synthesis of β-hydroxy-α-amino acid derivatives

Rahmani, Raphael,Matsumoto, Masatoshi,Yamashita, Yasuhiro,Kobayashi, Shu

, p. 1191 - 1194 (2012/07/28)

Two birds with one stone: Magnesium-base-catalyzed highly diastereoselective direct-type aldol reaction of glycine Schiff base bearing a fluorenylidene moiety as a protecting and activating group was developed. The desired reactions proceeded smoothly at low temperature, and the aldol products were obtained in high yield with high diastereoselectivity. Copyright

Methods for producing D-beta-hydroxyamino acids

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Page/Page column 12, (2008/06/13)

An objective of the present invention is to provide efficient methods for producing D-β-hydroxyamino acids (formula 2 or 4), such as D-erythro-2-amino-3-cyclohexyl-3-hydroxypropionic acid, which are useful as intermediates in the synthesis of pharmaceutical products and others. The present invention makes it possible to efficiently produce D-erythro-2-amino-3-cyclohexyl-3-hydroxypropionic acid by cleaving unnecessary L-erythro-2-amino-3-cyclohexyl-3-hydroxypropionic acid in industrially feasible concentrations of DL-erythro-2-amino-3-cyclohexyl-3-hydroxypropionic acid used as starting material by using Pseudomonas putida-derived L-phenylserine aldolase.

ENANTIOSPECIFIC AND DIASTEREOSELECTIVE SYNTHESIS OF ANTI α-HYDRAZINO- AND α-AMINO-β-HYDROXYACIDS THROUGH "ELECTROPHILIC AMINATION" OF β-HYDROXYESTERS

Guanti, Giuseppe,Banfi, Luca,Narisano, Enrica

, p. 5553 - 5562 (2007/10/02)

β-Hydroxyesters 1a-d were transformed into corresponding dianions and condensed with di-t-butylazodicarboxylate to give anti protected α-hydrazino-β-hydroxyesters 2a-d with good diastereoselectivities (up to 94:6).Cleavage of protecting groups followed by ester hydrolysis gave the previously unknown anti α-hydrazino-β-hydroxyacids 4a-d, which were in turn converted by hydrogenolysis into anti α-amino-β-hydroxyacids 5a-d.Starting from (S) 1a, enantiomerically pure (2S,3S) allo-threonine 5a was obtained in good overall yields.On the contrary, reaction of silyl ketene acetal 10, derived from 1a, with a diazonium salt furnished predominantly the syn isomer, but in unsatisfactory yield.

DIASTEREOSELECTIVE SYNTHESIS OF α-AMINO-β-HYDROXYACIDS

Guanti, Giuseppe,Banfi, Luca,Narisano, Enrica,Scolastico, Carlo

, p. 4693 - 4696 (2007/10/02)

threo-α-Dibenzylamino-β-hydroxyesters (2) have been synthesised with high diastereoselectivity through the reduction of α-dibenzylamino-β-oxoesters (4) and then transformed into threo-α-amino-β-hydroxyacids.

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