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
数量:
25 g
100 g
500 g
製品番号(カタログ番号) A11043.22
または、製品番号A11043-22
価格(JPY)
-
見積もりを依頼する
数量:
100 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS10191-60-3
IUPAC Name[bis(methylsulfanyl)methylidene](cyano)amine
Molecular FormulaC4H6N2S2
InChI KeyIULFXBLVJIPESI-UHFFFAOYSA-N
SMILESCSC(SC)=NC#N
さらに表示
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.