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609-08-5 | Diethyl Methylmalonate
CAS No: 609-08-5 Catalog No: AG003PGY MDL No:MFCD00009162
Product Description
Catalog Number:
AG003PGY
Chemical Name:
Diethyl Methylmalonate
CAS Number:
609-08-5
Molecular Formula:
C8H14O4
Molecular Weight:
174.1944
MDL Number:
MFCD00009162
IUPAC Name:
diethyl 2-methylpropanedioate
InChI:
InChI=1S/C8H14O4/c1-4-11-7(9)6(3)8(10)12-5-2/h6H,4-5H2,1-3H3
InChI Key:
UPQZOUHVTJNGFK-UHFFFAOYSA-N
SMILES:
CCOC(=O)C(C(=O)OCC)C
EC Number:
210-175-7
UNII:
7KD9S8CQN2
NSC Number:
8700
Properties
Complexity:
146
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
174.089g/mol
Formal Charge:
0
Heavy Atom Count:
12
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
174.196g/mol
Monoisotopic Mass:
174.089g/mol
Rotatable Bond Count:
6
Topological Polar Surface Area:
52.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.4
Literature
| Title | Journal |
|---|---|
| An erythromycin process improvement using the diethyl methylmalonate-responsive (Dmr) phenotype of the Saccharopolyspora erythraea mutB strain. | Applied microbiology and biotechnology 20120201 |
| 1-Butyl-4-hy-droxy-3-methyl-quinoline-2(1H)-one. | Acta crystallographica. Section E, Structure reports online 20101201 |
| A Cu2+ ion-selective fluoroionophore with dual off/on switches. | Chemistry Central journal 20100101 |
| NMR spectroscopy and MALDI-TOF MS characterisation of end-functionalised PVP oligomers prepared with different esters as chain transfer agents. | Macromolecular bioscience 20060314 |
| Bulky monodentate phosphoramidites in palladium-catalyzed allylic alkylation reactions: aspects of regioselectivity and enantioselectivity. | Chemistry (Weinheim an der Bergstrasse, Germany) 20041203 |
| Selective addition to [60]fullerene of two different radicals generated from Mn(III)-based radical reaction. | Organic & biomolecular chemistry 20040421 |
| Formal synthesis of angiogenesis inhibitor NM-3. | The Journal of organic chemistry 20030725 |
| Acylation through Ketene Intermediates. | The Journal of organic chemistry 20021213 |
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