54280-70-5 Usage
Uses
Used in Flavoring Industry:
3-FURYL(OXO)ACETIC ACID is used as a flavoring agent for its distinctive sweet, fruity scent, enhancing the taste and aroma of various food products.
Used in Organic Synthesis:
3-FURYL(OXO)ACETIC ACID is utilized as a building block in the synthesis of various organic compounds, contributing to the development of new chemical entities.
Used in Pharmaceutical Development:
3-FURYL(OXO)ACETIC ACID is used as a key component in the creation of pharmaceuticals, potentially leading to the discovery of new drugs and treatments.
Used in Agrochemical Production:
3-FURYL(OXO)ACETIC ACID is employed in the development of agrochemicals, which can be used in agriculture to protect crops and enhance yields.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, 3-FURYL(OXO)ACETIC ACID is used in applications that require the inhibition of microbial growth, contributing to food preservation and hygiene.
Used in Antioxidant Formulations:
Leveraging its antioxidant characteristics, 3-FURYL(OXO)ACETIC ACID is used in formulations that help prevent oxidative damage and support overall health.
Check Digit Verification of cas no
The CAS Registry Mumber 54280-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,8 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54280-70:
(7*5)+(6*4)+(5*2)+(4*8)+(3*0)+(2*7)+(1*0)=115
115 % 10 = 5
So 54280-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H4O4/c7-5(6(8)9)4-1-2-10-3-4/h1-3H,(H,8,9)
54280-70-5Relevant academic research and scientific papers
Direct Synthesis of N-Alkyl Arylglycines by Organocatalytic Asymmetric Transfer Hydrogenation of N-Alkyl Aryl Imino Esters
Mazuela, Javier,Antonsson, Thomas,Johansson, Magnus J.,Knerr, Laurent,Marsden, Stephen P.
supporting information, p. 5541 - 5544 (2017/10/25)
The organocatalytic asymmetric transfer hydrogenation of N-alkyl aryl imino esters for the direct synthesis of N-alkylated arylglycinate esters is reported. High yields and enantiomeric ratios were obtained, and tolerance to a diverse set of functional groups facilitated the preparation of more complex molecules as well as intermediates for active pharmaceuticals. A simple recycling protocol was developed for the Br?nsted acid catalyst which could be reused through five cycles with no loss of activity or selectivity.
Preparation of 2-aryl-2-hydroxyiminoacetic acids (syn isomers)
-
, (2008/06/13)
2-Aryl-2-hydroxyiminoacetic acids rich in the syn isomer are prepared by reaction of an arylglyoxylic acid with hydroxylamine in an aqueous reaction medium, e.g. water, in the presence of a source of magnesium, calcium or zinc ions, e.g. magnesium hydroxi
