Dimethylthiocarbamoyl chloride, 95%, Thermo Scientific Chemicals
Dimethylthiocarbamoyl chloride, 95%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Dimethylthiocarbamoyl chloride, 95%, Thermo Scientific Chemicals

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Quantity:
25 g
100 g
Catalog number H60104.14
also known as H60104-14
Price (USD)/ Each
71.65
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79.10 
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Quantity:
25 g
Request bulk or custom format
Price (USD)/ Each
71.65
Online exclusive
79.10 
Save 7.45 (9%)
Add to cart
Dimethylthiocarbamoyl chloride, 95%, Thermo Scientific Chemicals
Catalog numberH60104.14
Price (USD)/ Each
71.65
Online exclusive
79.10 
Save 7.45 (9%)
-
Add to cart
Chemical Identifiers
CAS16420-13-6
IUPAC Name(chloromethanethioyl)dimethylamine
Molecular FormulaC3H6ClNS
InChI KeyPHWISQNXPLXQRU-UHFFFAOYSA-N
SMILESCN(C)C(Cl)=S
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SpecificationsSpecification SheetSpecification Sheet
Proton NMR94.0% min
Dimethylthiocarbamoyl chloride is used as an intermediate in the synthesis of pharmaceuticals. It finds application in chemoselective deoxygenation of pyridine-N-oxides. It is also used as a starting reagent in the synthesis of dimethylthiocarbamates.

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
Dimethylthiocarbamoyl chloride is used as an intermediate in the synthesis of pharmaceuticals. It finds application in chemoselective deoxygenation of pyridine-N-oxides. It is also used as a starting reagent in the synthesis of dimethylthiocarbamates.

Solubility
Soluble in chloroform and tetrahydrofuran.

Notes
Store in cool place. Moisture sensitive. Incompatible with strong oxidizing agents, amines and strong bases. Reacts violently with water.
WARNING: Cancer – www.P65Warnings.ca.gov
RUO – Research Use Only

General References:

  1. Zaim, O.; Tuzun, N. S.; Cevik, B.; Ozcan, H.; Boz, E. Synthesis, reactions and DFT study of tropolone N,N-dimethylthiocarbamate. Tetrahedron 2015, 71 (33), 5391-5398.
  2. Gandhi, M. R.; Yamada, M.; Kondo, Y.; Sato, R.; Hamada, F. Synthesis and Characterization of Dimethylthiocarbamoyl-Modified Thiacalix[n]arenes for Selective Pd(II)-Ion Extraction. Ind. Eng. Chem. Res. 2014, 53 (7), 2559-2565.