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diphenylmercury(II)
trimethyl gallium
A
methyl(diphenyl)gallium
B
dimethylmercury
Conditions | Yield |
---|---|
In neat (no solvent) (CH3)3Ga was added to freshly sublimed diphenylmercury, the suspn. was heated at 100°C in a closed vessel for 3 h, cooled to room temp. without stiring; volatiles were removed in vac. (1E-2 mbar), crystals were washed with n-hexane and dried in vac. for 2 h: elem. anal.; | A 98% B n/a |
bis(trifluoromethyl)mercury
Tetramethylblei-(IV)
A
dimethylmercury
B
methyl(trifluoromethyl)mercury
C
trimethyl(trifluoromethyl)lead
Conditions | Yield |
---|---|
In toluene absence of air and moisture; heating of PbMe4 with two-fold excess of Hg-compd. (sealed tube, 70°C, 2 weeks); gas chromy.; | A 2% B 94% C 93% |
diphenylmercury(II)
trimethyl gallium
A
dimethyl(phenyl)gallium
B
dimethylmercury
Conditions | Yield |
---|---|
In neat (no solvent) in an Schlenk flask (CH3)3Ga was added to freshly sublimed (C6H5)2Hg, the vessel was tightly closed, the suspn. was heated at 100°C for 5h, cooled to room temp.; volatiles were removed under reduced pressure (10 mbar), the residue waswashed twice with n-hexane at -70°C; elem. anal.; | A 90% B n/a |
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: methylchloride; 23°C, 12 equiv of methylmagnesiumchloride; | A 85% B n/a |
[(C5H5)2Ti(C6H5)(CH3)]
methylmercury(II) chloride
A
bis(cyclopentadienyl)methyltitanium(IV) chloride
C
dimethylmercury
D
methyl phenyl mercury
Conditions | Yield |
---|---|
In [(2)H6]acetone to cold (-78 °C) soln. of Ti complex (excess) in acetone-d6 added soln. of MeHgCl in acetone-d6 under N2, stirred at -78 °C for 2h, stirred at room temp. for 6 h; monitored by NMR; | A 40% B 60% C 60% D 40% |
1-(2-hydroxyethyl)-3-methyl-(1H)-imidazole-2(3H)-selone
methylmercury(II) chloride
B
dimethylmercury
Conditions | Yield |
---|---|
In water; acetonitrile at 23℃; for 168h; Kinetics; Schlenk technique; | A 53% B n/a |
A
GLUTATHIONE
C
dimethylmercury
D
1-(2-hydroxyethyl)-3-methyl-1H-benzo[d]imidazol-2(3H)-one
Conditions | Yield |
---|---|
Stage #1: methylmercury-L-glutathionate; 1-(2-hydroxyethyl)-3-methyl-1H-benzo[d]imidazole-2(3H)-thione In water; acetonitrile at 37℃; for 1h; Stage #2: With sodium hydrogencarbonate In water; acetonitrile at 37℃; for 5h; | A n/a B 11 mg C n/a D 40% |
Conditions | Yield |
---|---|
With sodium amalgam; acetic acid methyl ester at -5 - -3℃; |
Conditions | Yield |
---|---|
With diethyl ether; mercury dichloride |
Conditions | Yield |
---|---|
With mercury |
Dimethylmercury is most often used in toxicology experiments as a fixed point of reference due to its extreme toxicity. It has also been used to calibrate NMR instruments for detection of mercury, although less toxic mercury salts are preferred.
1. | dnd-mmo-omi 600 mg/L | NATUAS Nature. 257 (1975),422. | ||
2. | oth-mus:oth 25 mg/L | MUREAV Mutation Research. 17 (1973),93. |