Molecule:100529
From ChemWiki
molecule
| Properties | |
|---|---|
| CID | 6228 |
| CAS | 68-12-2 |
| IUPAC-Name | N,N-dimethylmethanamide |
| Abbreviation | DMF |
| Trivialname | N,N-DIMETHYLFORMAMIDE |
| Exact mass | 73.052763847 |
| Molecular formula | C3H7NO |
| LogP | -1 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | N,N-DIMETHYLFORMAMIDE, Dimethylformamide, N,N-Dimethylmethanamide, Dimethyl formamide, N-Formyldimethylamine, Formamide, N,N-dimethyl-, Dimethylformamid, DMF, Dimetilformamide, Dwumetyloformamid, DMFA, Formyldimethylamine, N,N-Dimethyl formamide, Dimethylforamide, Dimetylformamidu, DMF (amide), NCI-C60913, dimethyl-Formamide, n,n,dimethylformamide, Dimethylamid kyseliny mravenci, U-4224, n,n-dimethyl-Formamide, N, N-dimethylformamide, N,N- Dimethylformamide, N,N-Dimethylformaldehyde, MFCD00003284, DTXSID6020515, CHEBI:17741, NSC5356, 8696NH0Y2X, NSC-5356, DSSTox_CID_515, DSSTox_RID_75636, DSSTox_GSID_20515, N,N-Dimethylformamid, N,N Dimethylformamide, Caswell No. 366A, N,N-Dimethylformamide, HPLC Grade, [[Synonym::Dimetylformamidu [Czech]]], [[Synonym::Dimethylformamid [German]]], [[Synonym::Dimetilformamide [Italian]]], [[Synonym::Dwumetyloformamid [Polish]]], CAS-68-12-2, HSDB 78, N,N-Dimetilformamida, CCRIS 1638, [[Synonym::N,N-Dimetilformamida [Spanish]]], N,N-Dimethylformamide, for HPLC, >=99.9%, N,N-Dimethylformamide, ACS reagent, >=99.8%, N, N-dimethyl formamide, NSC 5356, Formic acid, amide, N,N-dimethyl-, EINECS 200-679-5, UN2265, [[Synonym::Dimethylamid kyseliny mravenci [Czech]]], EPA Pesticide Chemical Code 366200, dimethlforamide, dimethlformamide, dimethyformamide, dimetylformamide, UNII-8696NH0Y2X, dimehtylformamide, dimethlyformamide, dimethyiformamide, AI3-03311, dimethy formamide, dimethy1formamide, dimethyl foramide, dimethyl formamid, dimehtylformarnide, dimethylformarnide, dimethylforrnamide, dirnethylformamide, di-methylformamide, dimethylf ormamide, dimethylform amide, dimethylform-amide, dimethylformamid e, dimethylformamide-, dirnethylformarnide, n-dimethylformamide, dimethyl form-amide, dimethyl- formamide, dimethylfor- mamide, DMF,SP Grade, N,n-dimethylforamide, formamide, dimethyl-, N,N-dimethlformamide, N,N-dimethyformamide, N,N-dimetylformamide, n,n.dimethylformamide, N,N'dimethylformamide, N,N-dimethvlformamide, N.N-dimethylformamide, HCONMe2, Formamide,N-dimethyl-, N, N-dimethylforamide, N,N'-dimethylforamide, N,N-dimethl formamide, N,N-dimethy formamide, N,N-dimethyl foramide, N,N-dimethyl formamid, N,N-dimethylformarnide, N,N-dimethylforrnamide, N,N-dimetyl formamide, N,N-dirnethylformamide, n,n,-dimethylformamide, Dimethylformamide, DMF, DMF, Dimethylformamide, N, N dimethylformamide, N,N -dimethylformamide, N,N dimethyl formamide, N,N' dimethylformamide, N,N-di methylformamide, N,N-di-methylformamide, N,N-dime-thylformamide, N,N-dimehtyl formamide, N,N-dimethylfor mamide, N,N-dimethylfor-mamide, N,N-dimethylform-amide, N,N-dimethylformamide-, N,N-di-methylforrnamide, Dimethyl Fornamide,(S), DMF (dimethylformamide), n,n,-dimethyl formamide, N, N'-dimethylformamide, N, N- dimethylformamide, N, N-di-methylformamide, N, N-dimethyl-formamide, N,N- dimethyl formamide, N,N-di-methyl formamide, N,N-di-methyl-formamide, N,N-dimethyl -formamide, N,N-dimethyl- formamide, N, N-dimethylformaldehyde, bmse000709, EC 200-679-5, D.M.F, HCON(CH3)2, Dynasolve 100 (Salt/Mix), BIDD:ER0600, WLN: VHN1&1, CHEMBL268291, D.M.F., N,N-Dimethylformamide, 99.8%, N,N-Dimethylformamide, anhydrous, N,N-Dimethylformamide HPLC grade, N,N-Dimethylformamide, ACS grade, ZINC901648, Dimethylformamide Reagent Grade ACS, Tox21_201259, Tox21_300039, N,N-Dimethylformamide, biotech grade, s6192, STL264197, N,N-Dimethylformamide, LR, >=99%, AKOS000121096, FORMIN ACID,AMIDE,N,N-DIMETHYL, DB01844, UN 2265, N,N-Dimethylformamide, p.a., 99.8%, N,N-Dimethylformamide, AR, >=99.5%, NCGC00090785-01, NCGC00090785-02, NCGC00090785-03, NCGC00090785-04, NCGC00090785-05, NCGC00254093-01, NCGC00258811-01, Dimethylformamide, n,n- Reagent Grade ACS, N,N-Dimethylformamide, analytical standard, N,N-Dimethylformamide, anhydrous, 99.8%, D0722, D0939, FT-0629532, FT-0629533, FT-0639029, FT-0696040, N,N-Dimethylformamide, anhydrous, amine free, N,N-Dimethylformamide, for HPLC, >=99.5%, C03134, N,N-Dimethylformamide, Spectrophotometric Grade, N,N-Dimethylformamide, AldraSORB(TM), 99.8%, N,N-Dimethylformamide, ReagentPlus(R), >=99%, A836012, N,N-Dimethylformamide 1000 microg/mL in Methanol, N,N-Dimethylformamide, biotech. grade, >=99.9%, Q409298, N,N-Dimethylformamide, p.a., ACS reagent, 99.8%, N,N-Dimethylformamide, SAJ first grade, >=99.0%, [[Synonym::N,N-Dimethylformamide [UN2265] [Flammable liquid]]], N,N-Dimethylformamide 100 microg/mL in Acetonitrile, N,N-Dimethylformamide, anhydrous, ZerO2(TM), 99.8%, N,N-Dimethylformamide, for molecular biology, >=99%, N,N-Dimethylformamide, JIS special grade, >=99.5%, N,N-Dimethylformamide, UV HPLC spectroscopic, 99.7%, N,N-Dimethylformamide, ACS spectrophotometric grade, >=99.8%, N,N-Dimethylformamide HPLC, UV-IR min. 99.9%, isocratic grade, N,N-Dimethylformamide, B&J Brand (product of Burdick & Jackson), N,N-Dimethylformamide, Vetec(TM) reagent grade, anhydrous, >=99.8%, Dimethylformamide, Pharmaceutical Secondary Standard; Certified Reference Material, N,N-Dimethylformamide, p.a., ACS reagent, reag. ISO, reag. Ph. Eur., 99.8%, N,N-Dimethylformamide, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.8% (GC), N,N-Dimethylformamide, suitable for neutral marker for measuring electroosmotic flow (EOF), ~99% |
Click here to copy MOL-file.
Click here to show SMILES and InChI.
Molecule is used on following pages
topic
- Photocatalytic CO2 conversion to CO
- Homogeneous photocatalytic CO2 conversion
- Photocatalytic CO2 conversion to HCOOH
- Photocatalytic CO2 conversion to CH4
publication
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production
- Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer
- 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
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
investigation
- Visible-Light-Driven Photocatalytic CO2 Reduction by a Ni(II) Complex Bearing a Bioinspired Tetradentate Ligand for Selective CO Production/Table 1
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH/Table 1
- Photocatalytic CO2 reduction using a Mn complex as a catalyst/Photocatalytic CO2 reduction: conditions optimization
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 1
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 2
- Exploring the Full Potential of Photocatalytic Carbon Dioxide Reduction Using a Dinuclear Re2Cl2 Complex Assisted by Various Photosensitizers/Optimizations of the conditions
- Nickel(II) pincer complexes demonstrate that the remote substituent controls catalytic carbon dioxide reduction/Photocatalytic CO2 reduction under varied conditions
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore/Photocatalytic CO2 reduction: best results
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction/Table 1
- Rhenium(I) trinuclear rings as highly efficient redox photosensitizers for photocatalytic CO2 reduction/Table 2
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO2
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst/Photocatalytic reduction of CO
- Visible-Light Photocatalytic Reduction of CO2 to Formic Acid with a Ru Catalyst Supported by N,N’- Bis(diphenylphosphino)-2,6-diaminopyridine Ligands/Table 1
- Promoting photocatalytic CO2 reduction with a molecular copper purpurin chromophore/Control experiments
- Water-Assisted Highly Efficient Photocatalytic Reduction of CO2 to CO with Noble Metal-Free Bis(terpyridine)iron(II) Complexes and an Organic Photosensitizer/photocatalytic CO2 conversion
- Photocatalytic CO2 reduction with aminoanthraquinone organic dyes/Photocatalytic reduction of CO2 with different photosensitizers
- Photocatalytic CO2 reduction with aminoanthraquinone organic dyes/Photocatalytic CO2 reduction with varying concentrations of cat and PS
- 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/Time profile in DMF
- An integrated Re(I) photocatalyst and sensitizer that activates the formation of formic acid from reduction of CO2/Effect of proton donor
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Co(qpy)(H2O)2(ClO4)2 and purpurin
- Highly Efficient and Selective Photocatalytic CO2 Reduction by Iron and Cobalt Quaterpyridine Complexes/Optimizations of conditions for Fe(qpy)(H2O)2(ClO4)2
- Merging an organic TADF photosensitizer and a simple terpyridine–Fe(iii) complex for photocatalytic CO2 reduction/photocatalytic reduction of CO2 to CO
other
