Conditions | Yield |
---|---|
In water reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.; | 96% |
Conditions | Yield |
---|---|
In ethanol reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.; | 96% |
Conditions | Yield |
---|---|
In water reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.; | 95% |
Glutamic acid
DL-methionine-S-methylsulfonium chloride
(aquachloro-S-methylmethionato)(glutaminato)-O,O'-zinc
Conditions | Yield |
---|---|
In water reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.; | 93% |
chloride
DL-methionine-S-methylsulfonium chloride
A
methyl bromide
B
methylene chloride
C
methyl iodide
Conditions | Yield |
---|---|
With sea salt; dihydrogen peroxide; potassium carbonate In phosphate buffer Methylation; |
bromide
DL-methionine-S-methylsulfonium chloride
A
methyl bromide
B
methyl iodide
Conditions | Yield |
---|---|
With sea salt; dihydrogen peroxide; potassium carbonate In phosphate buffer Methylation; |
iodide
DL-methionine-S-methylsulfonium chloride
A
methyl bromide
B
methyl iodide
Conditions | Yield |
---|---|
With sea salt; dihydrogen peroxide; potassium carbonate In phosphate buffer Methylation; |
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
With hydrogenchloride; sodium nitrite |
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
In not given room temp.; |
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
In not given heating (67-70°C, 3 h); |
Conditions | Yield |
---|---|
In acetone |
Conditions | Yield |
---|---|
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.; |
nickel(II) carbonate
Glutamic acid
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
In water addn. of basic NiCO3 to equimolar quantities of the ligands dissolved in water; filtration, salting-out by repeated treating with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.; |
Conditions | Yield |
---|---|
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.; |
Conditions | Yield |
---|---|
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.; |
Conditions | Yield |
---|---|
In water addn. of FeCl3*6H2O to a mixt. of vitamin U and S-methyl-L-cysteine in water (molar ratio 1:1:2), addn. of LiCO3 in small portions, liberation of CO2; complex isolated from the soln. by addn. of a 1:1 mixt. of acetone and alcohol, oily ppt., treated with acetone to give a powder, washed with ether; elem. anal.; |
Conditions | Yield |
---|---|
In water react. with ZnO with stirring until dissolution of the ZnO; salting-out with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In water addn. of basic NiCO3 to equimolar quantities of the ligands dissolved in water; filtration, salting-out by repeated treating with acetone, elem. anal.; |
nickel(II) carbonate
DL-methionine-S-methylsulfonium chloride
aspartic Acid
Conditions | Yield |
---|---|
In water addn. of basic NiCO3 to equimolar quantities of the ligands dissolved in water; filtration, salting-out by repeated treating with acetone, elem. anal.; |
Conditions | Yield |
---|---|
In water addn. of vitamin U and S-methyl-L-cysteine to metal hydroxide in water (molar ratio 2:1:1), stirred to give a soln.; addn. of acetone; elem. anal.; |
Conditions | Yield |
---|---|
In water addn. of Fe(OH)3 to a mixt. of vitamin U and S-methyl-L-cysteine in water (molar ratio 1:1:2); complex isolated from the soln. by addn. of a 1:1 mixt. of acetone and alcohol, oily ppt., treated with acetone to give a powder, washed with ether; elem. anal.; |
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
In water addn. of vitamin U and cysteine to metal hydroxide in water (molar ratio 1:2:1), stirred (6 d), loose ppt.; sepn. of the ppt. from the supernatant liquid, treated with acetone, when it became viscous, treated with acetone to give a powder, washed with ether; elem. anal.; |
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
In water addn. of vitamin U and cysteine to metal hydroxide in water (molar ratio 2:1:1), stirred (6 d), loose ppt.; sepn. of the ppt. from the supernatant liquid, treated with acetone, when it became viscous, treated with acetone to give a powder, washed with ether; elem. anal.; |
DL-methionine-S-methylsulfonium chloride
Conditions | Yield |
---|---|
In water addn. of vitamin U and cysteine to metal hydroxide in water (molar ratio 1:1:1), stirred (4 d), pptn.; treatment with acetone; elem. anal.; |
The Sulfonium,(3-amino-3-carboxypropyl)dimethyl-, chloride (1:1), with the cas registry number 3493-12-7, has the IUPAC name of (3-amino-4-hydroxy-4-oxobutyl)-dimethylsulfanium chloride. And its product categories are including Iodonium Sulfonium & Oxonium Compounds; Sulfonium Compounds.
The characteristics of this kind of chemical are as follows: (1)#H bond acceptors: 3; (2)#H bond donors: 3; (3)#Freely Rotating Bonds: 5; (4)Polar Surface Area: 63.32; (5)Exact Mass: 199.043377; (6)MonoIsotopic Mass: 199.043377; (7)Topological Polar Surface Area: 64.3; (8)Heavy Atom Count: 11; (9)Complexity: 116; (10)Undefined Atom StereoCenter Count: 1; (11)Covalently-Bonded Unit Count: 2.
Additionally, the following datas could be converted into the molecular structure:
(1)Canonical SMILES: C[S+](C)CCC(C(=O)O)N.[Cl-]
(2)InChI: InChI=1S/C6H13NO2S.ClH/c1-10(2)4-3-5(7)6(8)9;/h5H,3-4,7H2,1-2H3;1H
(3)InChIKey: MYGVPKMVGSXPCQ-UHFFFAOYSA-N
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