281867
Diethyl acetamidomalonate-2-13C
≥99 atom % 13C, ≥99% (CP)
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About This Item
Linear Formula:
CH3CONH13CH(CO2C2H5)2
CAS Number:
Molecular Weight:
218.21
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
Recommended Products
isotopic purity
≥99 atom % 13C
Assay
≥99% (CP)
form
solid
bp
185 °C/20 mmHg (lit.)
mp
95-98 °C (lit.)
mass shift
M+1
SMILES string
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
InChI key
ISOLMABRZPQKOV-CDYZYAPPSA-N
Packaging
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Sambasivarao Kotha et al.
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.
Soraia Veloso Silva Santana et al.
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
G K Powell et al.
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
Zsolt Rapi et al.
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
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