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Merck
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Key Documents

281867

Sigma-Aldrich

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 코드:
12352202
PubChem Substance ID:

동위원소 순도

≥99 atom % 13C

분석

≥99% (CP)

형태

solid

bp

185 °C/20 mmHg (lit.)

mp

95-98 °C (lit.)

질량 이동

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

포장

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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문서 라이브러리 방문

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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