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Key Documents

D84601

Sigma-Aldrich

Diethyl acetamidomalonate

98%

Synonym(s):

Acetamidomalonic acid diethyl ester

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About This Item

Linear Formula:
CH3CONHCH(CO2C2H5)2
CAS Number:
Molecular Weight:
217.22
Beilstein:
783883
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

powder

bp

185 °C/20 mmHg (lit.)

mp

95-98 °C (lit.)

SMILES string

CCOC(=O)C(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)

InChI key

ISOLMABRZPQKOV-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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