Dimethyl cyanodithioiminocarbonate, 95%
Dimethyl cyanodithioiminocarbonate, 95%
Dimethyl cyanodithioiminocarbonate, 95%
Dimethyl cyanodithioiminocarbonate, 95%
Thermo Scientific Chemicals

Dimethyl cyanodithioiminocarbonate, 95%

CAS: 10191-60-3 | C4H6N2S2 | 146.226 g/mol
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產品號碼 A11043.22
亦稱為 A11043-22
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化學識別
CAS10191-60-3
IUPAC Name[bis(methylsulfanyl)methylidene](cyano)amine
Molecular FormulaC4H6N2S2
InChI KeyIULFXBLVJIPESI-UHFFFAOYSA-N
SMILESCSC(SC)=NC#N
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規格Specification Sheet規格表
Appearance (Color)White to yellow or pale brown
FormPowder and/or Lumps
Assay (GC)>94.0%
Water Content (Karl Fischer Titration)<2.0%
Dimethyl 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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Dimethyl 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.

Solubility
Slightly soluble in methanol.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Yong-Qian Wu; Sean K.Hamilton; Douglas E.Wilkinson; Gregory S.Hamilton. Direct synthesis of guanidines using Di(imidazole-1-yl)methanimine. J. Org. Chem. 2002, 67,(21), 7553-7556.
  2. Aiguo Zhang; Hartmut Kaiser; Peter Maienfisch; John E.Casida. Insect nicotinic acetylcholine receptor: Conserved neonicotinoid specificity of [3H]imidacloprid binding site. Journal of Neurochemistry. 2000, 75,(3), 1294-1303.