N-Cyanoimido-S,S-dimethyl-dithiocarbonate

N-Cyanoimido-S,S-dimethyl-dithiocarbonate Basic information
Product Name:N-Cyanoimido-S,S-dimethyl-dithiocarbonate
Synonyms:s,s-dimethyl cyanoimidodithiocarbonate;S,S'-DIMETHYL N-CYANODITHIOIMINOCARBONATE;N-CYANO-S,S'-DIMETHYLDITHIOIMIDOCARBONATE;N-CYANO-S,S-DIMETHYLDITHIOIMIDOCARBONATE;N-CYANOIMIDO-S,S-DIMETHYL-DITHIOCARBONATE;(Cyanoimino)bis(methylthio)methane;Carbonimidodithioic acid, cyano-, dimethyl ester;Carbonimidodithioicacid,cyano-,dimethylester
CAS:10191-60-3
MF:C4H6N2S2
MW:146.23
EINECS:233-467-6
Product Categories:Pharmaceutical Intermediate;organic chemical;Organic Building Blocks;Others;Sulfur Compounds;Pharmaceutical Intermediates
Mol File:10191-60-3.mol
N-Cyanoimido-S,S-dimethyl-dithiocarbonate Structure
N-Cyanoimido-S,S-dimethyl-dithiocarbonate Chemical Properties
Melting point 45-50 °C (lit.)
Boiling point 229.6±23.0 °C(Predicted)
density 1.298 (estimate)
refractive index 1.5000 (estimate)
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
solubility Slightly soluble in methanol.
form solid
pka-5.10±0.50(Predicted)
BRN 635998
InChIKeyIULFXBLVJIPESI-UHFFFAOYSA-N
CAS DataBase Reference10191-60-3(CAS DataBase Reference)
NIST Chemistry ReferenceN-Cyano-s,s'-dimethyldithioimido carbonate(10191-60-3)
EPA Substance Registry SystemCarbonimidodithioic acid, cyano-, dimethyl ester (10191-60-3)
Safety Information
Hazard Codes C,T
Risk Statements 22-34-23/24/25-36/37
Safety Statements 26-36/37/39-45-38-28A-7/9
RIDADR UN 1759 8/PG 2
WGK Germany 3
13-19
TSCA Yes
HazardClass 6.1
PackingGroup II
HS Code 29309090
MSDS Information
ProviderLanguage
{[Bis(methylthio)methylene]amino}(nitrilo)methane English
SigmaAldrich English
ACROS English
ALFA English
N-Cyanoimido-S,S-dimethyl-dithiocarbonate Usage And Synthesis
Chemical Propertiesyellow crystalline powder
UsesDimethyl cyanodithioiminocarbonate has been used in the synthesis of 4-methylthiopyrazolo[1,5-a]-1,3,5-triazines, methylsulfanylpyrimidines, cyanoguanidines and N-aryl-6-methylsulfanyl-4-oxopyrimidine-5-carbonitriles. It has been also used in the synthesis of methylsulfanyl derivatives of azoloazines and azoloazoles.
1-BROMO-4-[3-(((CYANOIMINO)[(5,5-DICHLORO-2-METHYLPENTA-2,4-DIENYL)THIO]METHYL)THIO)ALLANOYL]BENZENE CYANOGEN Dacthal methane RARECHEM AL FG 0090 N-Cyanoimido-S,S-dimethyl-dithiocarbonate ALTRENOGEST RARECHEM AL FC 0010 N-(1,3-DITHIOLAN-2-YLIDEN)CYANAMIDE RARECHEM AL FD 0086 S,S'-Dimethyl dithiocarbonate ISOMETHIOZIN RARECHEM AL FF 0050 BENZYL [3-OXO-3-(4-METHYLPHENYL)PROP-1-ENYL]CYANOCARBONIMIDODITHIOATE Dimethyl Cyanoamino Di-tyiocarbonate Cyano RARECHEM AL FC 0011 RARECHEM AL FD 0087

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