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5-Phenyl-4,5-Dihydroisoxazole-3-Carboxylic Acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10313-27-6

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10313-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10313-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10313-27:
(7*1)+(6*0)+(5*3)+(4*1)+(3*3)+(2*2)+(1*7)=46
46 % 10 = 6
So 10313-27-6 is a valid CAS Registry Number.

10313-27-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-4,5-dihydro-1,2-oxazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4,5-dihydro-5-phenyl-3-isoxazolecarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10313-27-6 SDS

10313-27-6Relevant academic research and scientific papers

Synthesis of unnatural α-amino esters using ethyl nitroacetate and condensation or cycloaddition reactions

Gagnot, Glwadys,Hervin, Vincent,Coutant, Eloi P.,Desmons, Sarah,Baatallah, Racha,Monnot, Victor,Janin, Yves L.

supporting information, p. 2846 - 2852 (2018/11/27)

We report here on the use of ethyl nitroacetate as a glycine template to produce α-amino esters. This started with a study of its condensation with various arylacetals to give ethyl 3-aryl-2-nitroacrylates followed by a reduction (NaBH4 and then zinc/HCl) into α-amino esters. The scope of this method was explored as well as an alternative with arylacylals instead. We also focused on various [2 + 3] cycloadditions, one leading to a spiroacetal, which led to the undesired ethyl 5-(benzamidomethyl)isoxazole-3-carboxylate. The addition of ethyl nitroacetate on a 5-methylene-4,5-dihydrooxazole using cerium(IV) ammonium nitrate was also explored and the synthesis of other oxazole-bearing α-amino esters was achieved using gold(I) chemistry.

AZOCYCLIC INHIBITORS OF FATTY ACID AMIDE HYDROLASE

-

, (2011/06/26)

Disclosed are compounds of Formula 1, including all stereoisomers, N oxides, and salts thereof, wherein A, W, X, G, R1, R2, R3, R4, m and n are as defined in the disclosure. Also disclosed are pharmaceutical compositions containing the compounds of Formula 1 and methods for treating a disease or condition mediated by fatty acid amide hydrolase activity comprising applying a therapeutically effective amount of a compound or a composition of the invention

INDOLE AMIDE DERIVATIVES AND RELATED COMPOUNDS FOR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES

-

Page/Page column 159, (2010/12/29)

This invention provides novel compounds and the novel compounds for use as a medicine, more in particular for the prevention or treatment of neurodegenerative disorders, more specifically certain neurological disorders, such as disorders collectively known as tauopathies, and disorders characterised by cytotoxic α-synuclein amyloidogenesis. The present invention also relates to the use of said novel compounds for the manufacture of medicaments useful for treating such neurodegenerative disorders. The present invention further relates to pharmaceutical compositions including said novel compounds and to methods for the preparation of said novel compounds.

FUNGICIDAL MIXTURES

-

Page/Page column 66, (2010/10/03)

Disclosed is a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1 N-oxides, and salts thereof, wherein R1, R2, A, G, W, Z1, X, J, and n are as defined in the disclosure, and (b) at least one additional fungicidal compound. Also disclosed is a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of the aforesaid composition. Also disclosed is a composition comprising component (a) of aforesaid composition and at least one insecticide. Also disclosed are compounds of Formula 1A, 1B and 1C, wherein R1, R2, A, G, W, Z1, X, J, n, Z3, M and J1 are as defined in the disclosure.

Enzymatic resolution of (±)-5-phenyl-4,5-dihydroisoxazole-3-carboxylic acid ethyl ester and its transformations into polyfunctionalised amino acids and dipeptides

Cremonesi, Giuseppe,Croce, Piero Dalla,Forni, Alessandra,Gallanti, Maddalena,Gandolfi, Raffaella,La Rosa, Concetta

scheme or table, p. 1940 - 1947 (2010/01/16)

Enantiomerically pure (5R)-(-)-5-phenyl-4,5-dihydroisoxazole-3-carboxylic acid ethyl ester was obtained via enzymatic resolution of the corresponding racemic mixture using a lipase from hog pancreas (PPL). The following reduction of the ester group to the

ELECTRONIC COMPONENT HAVING FLEXIBLE PRINTED CIRCUIT BOARD TECHNOLOGY

-

, (2008/06/13)

The invention relates to an electronic component (1) having a housing comprising at least one base plate (3), a housing cover, and at least two electronic connections (5) between substrates (7) disposed in the interior of the housing and components located outside the housing in the form of printed circuit boards, which can be at least partially fixed on the base plate (3), wherein at least one first partially flexible printed circuit board (5a) and a second printed circuit board (5b) are configured such that they overlap at least in one region (6) in the assembled state. The invention further relates to a method for the production of such an electronic component.

Methods for the Stereoselective Cis Cyanohydroxylation and Carboxyhydroxylation of Olefins

Kozikowski, Alan P.,Adamczyk, Maciej

, p. 366 - 372 (2007/10/02)

Two valuable reagents for the cis-specific vicinal cyanohydroxylation and carboxyhydroxylation of olefins are described.The cyanohydroxylation process is based on the decarboxylative ring opening of 3-carboxyisoxazolines prepared by the cycloaddition reaction of carbethoxyformonitrile oxide with various alkenes.Fragmentation of the isoxazolines prepared from cis- and trans-2-butene has been found to occur without any crossover in stereochemistry.The carboxyhydroxylation process begins with the dipolar cycloaddition reaction of the nitrile oxide derived from thetetrahydropyranyl ether derivative of 2-nitroethanol.Deprotection, hydrogenation, and oxitative cleavage of the derived dihydroxy ketone yield the stereochemcally pure β-hydroxy carboxylic acid.

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