D84601
Diethyl acetamidomalonate
98%
Synonym(s):
Acetamidomalonic acid diethyl ester
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25 G
$42.90
100 G
$65.40
500 G
$181.30
About This Item
Linear Formula:
CH3CONHCH(CO2C2H5)2
CAS Number:
Molecular Weight:
217.22
Beilstein/REAXYS Number:
783883
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
powder
assay:
98%
Recommended Products
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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Related Categories
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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