carbon disulfide
N,N-dimethylammonium chloride
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 3h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide at 25℃; Temperature; | 99.85% |
With sodium hydroxide In water at 20℃; for 1.5h; Cooling with ice-water bath; | 59% |
With sodium hydroxide In methanol other reagent; |
Conditions | Yield |
---|---|
With sodium amalgam In tetrahydrofuran for 2h; |
Conditions | Yield |
---|---|
With water |
tetrachloromethane
N,N-dimethyl-formamide
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
With water |
N-benzyl-2,4,6-triphenylpyridinium tetrafluoroborate
sodium dimethyldithiocarbamate
benzyl dimethyldithiocarbamate
Conditions | Yield |
---|---|
In ethanol for 1h; Heating; | 99% |
sodium dimethyldithiocarbamate
S-butyl N,N-dimethyldithiocarbamate
Conditions | Yield |
---|---|
In water at 25℃; for 0.5h; | 99% |
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
In acetonitrile for 1h; Ambient temperature; | 99% |
1,2-dichloro-tetramethyl-distannane
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
In water to stirred soln. of tin compd. in degassed H2O was slowly added soln. of Na- (or NH4-) Me2NCSS (50-100% excess); formed ppt. was filtered off, washed with water, then with a little MeOH and dried in vac. at room temp.; recrystn. from CHCl3; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 0.5h; stereoselective reaction; | 99% |
Conditions | Yield |
---|---|
In dichloromethane; water at 25℃; for 1.5h; | 98% |
2-chloro-[1,3,2]dithiarsolane
sodium dimethyldithiocarbamate
2-Dimethyldithiocarbamato-1,3,2-dithioarsolan
Conditions | Yield |
---|---|
In benzene for 5h; Substitution; Heating; | 98% |
In ethanol for 5h; | 60% |
Conditions | Yield |
---|---|
In dichloromethane Kinetics; Stirring of mixt. of starting complexes in CH2Cl2 at reflux under anhydrous conditions in a dry Ar atmosphere (24 h).; Filtn. of react. mixt., removal of solvent by trap-to-trap distn., crystn. of crude resulting material from CH2Cl2 under hexane, elem. anal., variable-temp. NMR spectroscopy.; | A 98% B n/a |
dibromophenylbismuthane
sodium dimethyldithiocarbamate
Bis-(dimethyldithiocarbamato)-phenyl-bismut
Conditions | Yield |
---|---|
In chloroform | 98% |
In chloroform molar ratio sodium dimethylditiocarbamate:thiophenol = 2:1, 1 h, 25°C; recrystd. from CH3CN; | 98% |
In chloroform | 98% |
[((C6H5)2PCH2)2W(CCH2C6H5)(CO)2](1+)*BF4(1-)=((C6H5)2PCH2CH2P(C6H5)2)W(CCH2C6H5)(CO)2BF4
sodium dimethyldithiocarbamate
((CH3)2NCS2)((C6H5)2PCH2CH2P(C6H5)2)W(OCCCH2C6H5)(CO)(1+)*BF4(1-)
Conditions | Yield |
---|---|
In dichloromethane 1 equiv of Na salt adding to a soln. of the complex precooled to -23°C under N2, stirring for 0.5 h at -23°C, then 1.5 h at 0°C and 2 h at room temp., filtering, EtOH adding; purified by recrystallization from CH2Cl2-Et2O; identified by IR and NMR spectra; | 98% |
W(O)(CHC(CH3)3)Cl2(P(C2H5)3)2
sodium dimethyldithiocarbamate
W(O)(CHC(CH3)3)bis(dithiocarbamate)
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: NaCl; molar ratio W:Na=1:2, stirred for 2 d; filtered, solvent removed in vac., recrystd. from toluene/pentane, elem. anal.; | 98% |
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 0.166667h; stereoselective reaction; | 98% |
2-chlorocyclopentanone
sodium dimethyldithiocarbamate
2-(Dimethylamino-thiocarbonylthio)cyclopentanon
Conditions | Yield |
---|---|
In diethyl ether; acetone | 97% |
3-(trimethylsilyl)-2-oxoazetidin-4-yl acetate
sodium dimethyldithiocarbamate
(3S,4R)-3-(trimethylsilyl)-2-oxoazetidin-4-yl N,N-dimethyldithiocarbamate
Conditions | Yield |
---|---|
In water; acetone at 25℃; | 97% |
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
In acetonitrile at 80℃; for 1h; stereoselective reaction; | 97% |
sodium dimethyldithiocarbamate
{W(S2CN(CH3)2)2(OCC(C6H5)CHCHCH3)(CO)}
Conditions | Yield |
---|---|
In tetrahydrofuran under N2: addn. of NaS2CN(CH3)2 in THF to a slurry of allylidene tungsten in THF with stirring at 0°C; heating to 45-50°C for 1.5 h;; recrystallization by slow cooling of a satd. CH2Cl2/hexane soln. from ambient temperature to -78°C; mixture of 2 isomers;; | 96.5% |
1,2-dichloro-1,2-dimethoxyethane
sodium dimethyldithiocarbamate
Dimethyl-dithiocarbamic acid 2-dimethylthiocarbamoylsulfanyl-1,2-dimethoxy-ethyl ester
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide Ambient temperature; | 96% |
Conditions | Yield |
---|---|
In chloroform equimolar amts at 25°C; | 96% |
Conditions | Yield |
---|---|
With 1,3,5-trichloro-2,4,6-triazine; dimethyl sulfoxide In dichloromethane at 20℃; for 0.333333h; | 95% |
With hydrogenchloride; sodium nitrite In methanol; water at 0 - 5℃; for 0.333333h; | 56% |
In water at 25℃; Electrolysis; | 42% |
1N-methyl-2,4,6-triphenylpyridinium tetrafluoroborate
sodium dimethyldithiocarbamate
N,N,S-trimethyldithiocarbamate
Conditions | Yield |
---|---|
With 2,4,6-triphenylpyridine at 160℃; under 1 Torr; for 0.5h; | 95% |
5,5'-methylenebis(1-(2-bromoethyl)-3,6-dimethyl-2,4(1H,3H)-pyrimidinedione)
sodium dimethyldithiocarbamate
5,5'-methylenebis(3,6-dimethyl-1-(N,N-dimethylaminothiocarbonylthioethyl)-2,4(1H,3H)-pyrimidinedione)
Conditions | Yield |
---|---|
In methanol; chloroform for 2h; Heating; | 95% |
iodobenzene
sodium dimethyldithiocarbamate
phenyl N,N-dimethyl dithiocarbamate
Conditions | Yield |
---|---|
With dimethylaminoacetic acid; copper(l) iodide In N,N-dimethyl-formamide at 110℃; for 22h; Ullmann-type coupling; | 95% |
With copper diacetate; potassium carbonate In N,N-dimethyl-formamide at 120℃; for 6h; Sealed tube; | 87% |
dichlorophenylstibine
sodium dimethyldithiocarbamate
phenylantimony dimethyldithiocarbamate
Conditions | Yield |
---|---|
In chloroform at room temp.; | 95% |
[(μ-bis(diphenylphosphinomethyl)phenylphosphine)(AuCl)3 ]
sodium dimethyldithiocarbamate
(Au3(μ-bis(diphenylphosphinomethyl)phenylphosphine)(μ-S2CNMe2)Cl2)
Conditions | Yield |
---|---|
In dichloromethane under Ar atm. to CH2Cl2 suspn. ((μ-dpmp)(AuCl)3) was added NaS2CNMe2(1:1), soln. was stirred for 2 h; soln. was filtered, conc., hexane was added, solid was washed with hexane; elem. anal.; | 95% |
[(μ-bis(diphenylphosphinomethyl)phenylphosphine)(AuCl)3 ]
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
In dichloromethane under Ar atm. to CH2Cl2 suspn. ((μ-dpmp)(AuCl)3) was added NaS2CNMe2(1:2), soln. was stirred for 2 h; soln. was filtered, conc., hexane was added, solid was washed with hexane; elem. anal.; | 95% |
[(μ-bis(diphenylphosphinomethyl)phenylphosphine)(AuCl)3 ]
sodium dimethyldithiocarbamate
(Au3(μ-bis(diphenylphosphinomethyl)phenylphosphine)(μ-S2CNMe2)3)
Conditions | Yield |
---|---|
In dichloromethane under Ar atm. to CH2Cl2 suspn. ((μ-dpmp)(AuCl)3) was added NaS2CNMe2(1:3), soln. was stirred for 2 h; soln. was filtered, conc., Et2O was added, solid was washed with Et2O; elem. anal.; | 95% |
sodium dimethyldithiocarbamate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 150℃; for 2h; | 95% |
4-chloro-2-aminobenzenethiol
sodium dimethyldithiocarbamate
5-chloro-2-mercaptobenzothiazole
Conditions | Yield |
---|---|
With aluminum (III) chloride In water; N,N-dimethyl-formamide at 120℃; | 95% |
The IUPAC name of this chemical is Sodium N,N-dimethyldithiocarbamate. With the CAS registry number 128-04-1 and EINECS registry number 204-876-7, it is also named as Dimethyldithiocarbamicacid sodium salt. In addition, the molecular formula is C3H7NNaS2 and the molecular weight is 144.21. It is a kind of clear yellow solution and belongs to the classes of Pharmaceutical Intermediates; Aliphatics; Classes of Metal Compounds; Na (Sodium) Compounds (excluding simple sodium salts); Typical Metal Compounds. What's more, it can be used as intermediates in organic synthesis, accelerant of rubber, antiseptic and corrosion inhibitor.
Physical properties about this chemical are: (1)ACD/LogP: 0.75; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.06; (4)ACD/LogD (pH 7.4): -2.68; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 1; (10)#Freely Rotating Bonds: 0; (11)Polar Surface Area: 74.13 Å2; (12)Flash Point: 32 °C; (13)Enthalpy of Vaporization: 36.7 kJ/mol; (14)Boiling Point: 129.4 °C at 760 mmHg; (15)Vapour Pressure: 10.2 mmHg at 25°C.
When you are using this chemical, please be cautious about it as the following:
This chemical is harmful if swallowed and irritating to eyes. During using it, wear suitable protective clothing. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: [Na+].[S-]C(=S)N(C)C
(2)InChI: InChI=1/C3H7NS2.Na/c1-4(2)3(5)6;/h1-2H3,(H,5,6);/q;+1/p-1
(3)InChIKey: VMSRVIHUFHQIAL-REWHXWOFAU
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 573mg/kg (573mg/kg) | Yakugaku Zasshi. Journal of Pharmacy. Vol. 94, Pg. 1419, 1974. | |
mouse | LD50 | oral | 1500mg/kg (1500mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) | Farmakologiya i Toksikologiya Vol. 28, Pg. 230, 1965. |
rabbit | LD50 | oral | 300mg/kg (300mg/kg) | Toksikologicheskii Vestnik. Vol. (3), Pg. 34, 2000. | |
rat | LD | skin | > 5gm/kg (5000mg/kg) | Toksikologicheskii Vestnik. Vol. (3), Pg. 34, 2000. | |
rat | LD50 | intraperitoneal | 1gm/kg (1000mg/kg) | Pharmazie. Vol. 27, Pg. 139, 1972. | |
rat | LD50 | oral | 1gm/kg (1000mg/kg) | Pesticide Chemicals Official Compendium, Association of the American Pesticide Control Officials, Inc., 1966. Vol. -, Pg. 1029, 1966. |
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