% 200 at ca 442 nm in dimethylformamide
Maximum in dimethylformamide at ca 442 nm
dimethylformamide) and 3 (zinc chloride/formic acid
200 at ca. 442 nm in dimethylformamide
Maximum in dimethylformamide at ca. 442 nm
Pure Dimethylformamide is odorless, but industrial grade or modified Dimethylformamide has a fishy smell because it contains impurities of Dimethylamine.
The composite film has a content soluble in N,N-dimethylformamide (DMF).
3S)-3-[2-(mesyloxy)ethoxy]-4-(trityloxy)butyl methanesulfonate, dimethylformamide solution
8. (dimethylformamide) and 14. (concentrated sulphuric acid)
8. (dimethylformamide) and 14. (concentrated sulphuric acid)
Also disclosed are the 1,2-dichloroethane solvate of SnET2 and the N,N-dimethylformamide solvate of SnET2.
However, when using dimethylamine in this manner, a considerable amount of N,N-dimethylformamide was produced as a co-product.
Membrane films were cast from solution in N,N-dimethylformamide or N,N-dimethylacetamide.
The amine organic solvent preferably has a relative permittivity of 6 or higher, and pyridine, N,N-dimethylformamide or the like can preferably be used.
Treatment of HL60 with N,N-dimethylformamide differentiates the cell line into activated neutrophils with strong phagocytic activity11.
The short chain fatty acid amide comprises dimethyl formamide or Ν, Ν'-dimethyl acetamide.
3S)-3-[2-(mesyloxy)ethoxy]-4-(trityloxy)butyl methanesulfonate, dimethylformamide solution
As aprotic dipolar solvent dimethylformamide or N-methylpyrrolidinone is preferably chosen.
3-[2-(mesyloxy)ethoxy]-4-(trityloxy)butyl methanesulfonate, dimethylformamide solution
4. (formic acid 80 % m/m) and 8. (dimethylformamide)
Transfer any residual fibre to the crucible by washing out the beaker with dimethylformamide.
The catalyst may be dimethylformamide, (chloromethylene)dimethyliminium chloride, or triethylamine, among others.
4. (formic acid 80 % m/m) and 8. (dimethylformamide)
These compounds are obtained by reacting equi-molecular amounts of diaminodiphenylsulphone and 6-methyluracylsulphochloride in a dimethylformamide.
The present invention provides a process for the purification of norethindrone (I) from a mixture of dimethylformamide (DMF) and water.
Salt efflorescences of calcium carbonate were treated by the application of a solution of dimethylformamide.
Dimethylformamide (boiling point 153 ± 1 °C) not containing more than 0,1 % water.
Dimethylformamide (boiling point 153 ± 1 °C) not containing more than 0,1 % water.
Methods for the synthesis of 4,5-epoxy-morphinaniums using dimethyl formamide and resolution of the diastereomeric products by means of HPLC.
Dimethylformamide (boiling point 153 ± 1 °C) not containing more than 0,1 % water.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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