Molecule:100531
From ChemWiki
molecule
| Properties | |
|---|---|
| CID | 31374 |
| CAS | 127-19-5 |
| IUPAC-Name | N,N-dimethylethanamide |
| Abbreviation | DMA |
| Trivialname | N,N-DIMETHYLACETAMIDE |
| Exact mass | 87.068413911 |
| Molecular formula | C4H9NO |
| LogP | -0.8 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | N,N-DIMETHYLACETAMIDE, Dimethylacetamide, Acetamide, N,N-dimethyl-, DMAc, Acetdimethylamide, Dimethyl acetamide, N,N-Dimethyl acetamide, Dimethylamide acetate, N,N-Dimethylethanamide, Dimethylacetone amide, Acetic acid, dimethylamide, NSC 3138, N.N-Dimethylacetamide, Hallucinogen, CBC 510337, SK 7176, Dimethylamid kyseliny octove, MFCD00008686, Acetyl dimethylamine, U-5954, N, N-dimethylacetamide, N,N-Dimethyl-acetamide, JCV5VDB3HY, DTXSID5020499, CHEBI:84254, DSSTox_CID_499, Acetyldimethylamine, DSSTox_RID_75625, DSSTox_GSID_20499, CAS-127-19-5, HSDB 74, CCRIS 4623, N,N-dimethylacetoamide, UNII-JCV5VDB3HY, Acetic acid dimethylamide, [[Synonym::Dimethylamid kyseliny octove [Czech]]], EINECS 204-826-4, dimethyacetamide, dimethylactamide, N,N-Dimethylacetamide solution, dimethylacteamide, AI3-15276, trimethylformamide, dimeihyl acetamide, dimethyl-acetamide, n-dimethylacetamide, N,N-dimethyacetamide, N,N-dimethylactamide, N-Acetyldimethylamine, N,N dimethylacetamide, n,n,-dimethylacetamide, N,-N-dimethylacetamide, N,N -dimethylacetamide, N,N-di-methylacetamide, N,N-dimethylacet-amide, N, N-dimethylacetoamide, N,N-dimethyl acetoamide, DMAC, Dimethylacetamide, n,n,-dimethyl-acetamide, Acetic acid-dimethylamide, N,N-dimethyl- acetamide, EC 204-826-4, N,N-Dimethylacetamide solution (40% or less), N,N-dimethyl-N-acetylamine, CH3CON(CH3)2, N, N-Dimethylacetamide, EP, CHEMBL11873, N,N-Dimethylacetamide, >=99%, N,N-Dimethylacetamide, anhydrous, NSC3138, WLN: 1VN1 & 1, N,N-Dimethylacetamide, HPLC Grade, NSC-3138, ZINC1666602, Tox21_202174, Tox21_302787, STL482892, ACETIC ACID,AMIDE,N,N-DIMETHYL, AKOS000118789, [[Synonym::N,N-Dimethylacetamide-1,2-[13C2]]], CS-W023195, HY-W042416, N,N-Dimethylacetamide, p.a., 99.5%, N,N-Dimethylacetamide, AR, >=99.5%, NCGC00159401-02, NCGC00159401-03, NCGC00256375-01, NCGC00259723-01, BP-31151, N,N-Dimethylacetamide, SAJ special grade, N,N-Dimethylacetamide, analytical standard, N,N-Dimethylacetamide, anhydrous, 99.8%, DB-041302, D0641, FT-0629514, FT-0642826, N,N-Dimethylacetamide, for HPLC, >=99.7%, N,N-Dimethylacetamide, for HPLC, >=99.9%, N,N-Dimethylacetamide, ReagentPlus(R), 99%, C20339, N,N-Dimethylacetamide, ReagentPlus(R), >=99%, Q411452, Residual Solvent Class 2 - N,N-Dimethylacetamide, N,N-Dimethylacetamide, SAJ first grade, >=99.0%, N,N-Dimethylacetamide, UV HPLC spectroscopic, 99%, W-108388, N,N-Dimethylacetamide, anhydrous, ZerO2(TM), 99.8%, N,N-Dimethylacetamide, Vetec(TM) reagent grade, 98%, Z32014266, Acetic acid-dimethylamide 100 microg/mL in Acetonitrile, F0001-0392, N,N-Dimethylacetamide, puriss. p.a., >=99.5% (GC), N,N-Dimethylacetamide, spectrophotometric grade, >=99%, Acetic acid-dimethylamide 1000 microg/mL in Acetonitrile, N,N-Dimethylacetamide, for peptide synthesis, >=99.8% (GC), 5Y9, N,N-Dimethylacetamide, PharmaGrade, Manufactured under appropriate GMP controls for pharma and biopharmaceutical production., Ph Eur |
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Molecule is used on following pages
topic
- Photocatalytic CO2 conversion to CO
- Homogeneous photocatalytic CO2 conversion
- Photocatalytic CO2 conversion to HCOOH
publication
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid
- Photocatalytic CO2 Reduction under Visible-Light Irradiation by Ruthenium CNC Pincer Complexes
- Photocatalytic CO2 reduction using a Mn complex as a catalyst
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction
- Photocatalytic CO2 Reduction Mediated by Electron Transfer via the Excited Triplet State of Zn(II) Porphyrin
investigation
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid/Photocatalytic reduction of CO2, best TON
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production/Table 1
- Photocatalytic CO2 reduction using a Mn complex as a catalyst/Photocatalytic CO2 reduction: conditions optimization
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Control experiments
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Presence of water effect
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Hg poisoning
- Photocatalytic CO2 Reduction under Visible-Light Irradiation by Ruthenium CNC Pincer Complexes/Conditions optimizations for photocatalytic reduction of CO2
- Photocatalytic CO2 Reduction Using a Robust Multifunctional Iridium Complex toward the Selective Formation of Formic Acid/Control experiments
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Solvent effect study between DMA DMF and acetonitrile
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Study on the concentration of catalyst
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Concentration and solvent effect
- Function-Integrated Ru Catalyst for Photochemical CO2 Reduction/Maximum TON
- Photocatalytic CO2 Reduction Mediated by Electron Transfer via the Excited Triplet State of Zn(II) Porphyrin/photocatalytic CO2 conversion
other
