281867
Diethyl acetamidomalonate-2-13C
≥99 atom % 13C, ≥99% (CP)
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About This Item
Prodotti consigliati
Purezza isotopica
≥99 atom % 13C
Livello qualitativo
Saggio
≥99% (CP)
Forma fisica
solid
P. eboll.
185 °C/20 mmHg (lit.)
Punto di fusione
95-98 °C (lit.)
Spostamento di massa
M+1
Stringa SMILE
CCOC(=O)[13CH](NC(C)=O)C(=O)OCC
InChI
1S/C9H15NO5/c1-4-14-8(12)7(10-6(3)11)9(13)15-5-2/h7H,4-5H2,1-3H3,(H,10,11)/i7+1
ISOLMABRZPQKOV-CDYZYAPPSA-N
Categorie correlate
Confezionamento
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Certificati d'analisi (COA)
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Amino acids, 41(4), 933-936 (2010-11-10)
Strategically a new approach for the synthesis tetrahydro-β-carboline unit with the aid of diethyl acetamidomalonate as a glycine equivalent has been described.
Journal of esthetic and restorative dentistry : official publication of the American Academy of Esthetic Dentistry ... [et al.], 21(6), 397-404 (2009-12-17)
Surface sealants may reduce or avoid problems related to the marginal interface. The aim of this study was to evaluate the microleakage in resin composite Class V restorations sealed with an adhesive system (Xeno III [Dentsply, Konstanz, Germany]), a sealant
Carbohydrate research, 365, 61-68 (2012-12-12)
The synthesis of four new ribo-hexopyranoside-based chiral lariat ethers of monoaza-15-crown-5 type and two altropyranoside-based crown ethers were elaborated. Our syntheses utilized the regioselective ring opening of the oxiran moiety of the 2,3-anhydro sugars by nucleophilic reagents to afford the
Preparative biochemistry, 11(3), 339-350 (1981-01-01)
This paper describes the complete chemical synthesis of 4-methylene-DL-glutamic acid from diethylmalonate, formaldehyde and diethyl acetamidomalonate. The amino acid was obtained pure following ion-exchange chromatography and/or crystallization from hot water in an overall yield of 30% based on the amount
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