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Carbamic acid, [1-(4,5-dihydro-4,4-dimethyl-5-oxo-2-oxazolyl)-1-methylethyl]-, phenylmethyl ester is a complex organic compound with the chemical formula C14H17NO4. It is a derivative of carbamic acid, featuring a phenylmethyl ester group and a 4,5-dihydro-4,4-dimethyl-5-oxo-2-oxazolyl moiety. Carbamic acid, [1-(4,5-dihydro-4,4-dimethyl-5-oxo-2-oxazolyl)-1-methylethyl]-, phenylmethyl ester is characterized by its unique structure, which includes a cyclic oxazolyl ring and a methylethyl chain connected to the carbamic acid backbone. It is synthesized through a series of chemical reactions and is used in various applications, such as in the pharmaceutical industry for the development of drugs and agrochemicals. The compound's specific properties and reactivity are determined by its molecular structure, making it a subject of interest for chemists and researchers in related fields.

4576-16-3

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4576-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4576-16-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4576-16:
(6*4)+(5*5)+(4*7)+(3*6)+(2*1)+(1*6)=103
103 % 10 = 3
So 4576-16-3 is a valid CAS Registry Number.

4576-16-3Relevant academic research and scientific papers

Deracemization and the first CD spectrum of a 310-helical peptide made of achiral α-amino-isobutyric acid residues in a chiral membrane mimetic environment

Ceccacci, Francesca,Mancini, Giovanna,Rossi, Paola,Scrimin, Paolo,Sorrenti, Alessandro,Tecilla, Paolo

, p. 10133 - 10135 (2013/10/22)

Interaction of the racemic helical homo-octapeptide made by the achiral Cα-methyl alanine (Aib) amino acid with a chiral enantiopure micellar aggregate made of N-dodecylproline led to the deracemization of the helical Aib sequence thus allowing

Emerimicins III and IV and their ethylalanine12 epimers. Facilitated chemical-enzymatic synthesis and a qualitative evaluation of their solution structures

Slomczynska, Urszula,Beusen, Denise D.,Zabrocki, Janusz,Kociolek, Karol,Redlinski, Adam,Rensser, Fritz,Hutton, William C.,Leplawy, Miroslaw T.,Marshall, Garland R.

, p. 4095 - 4106 (2007/10/02)

The peptaibol antibiotics, emerimicin III and IV (Ac-Phe1-MeA2-MeA3-MeA4-VaI 5-Gly6-Leu7-MeA8-MeA 9-Hyp10-Gln11-R-EtA12-Hyp

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