Dimethylthiocarbamoyl chloride, 95%

Name: Dimethylthiocarbamoyl chloride, 95%
SKU: H60104.22

CAS: 16420-13-6 | C3H6ClNS | 123.60 g/mol

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25 g

100 g

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產品號碼 H60104.22

亦稱為 H60104-22

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100 g

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化學識別

CAS16420-13-6

IUPAC Name(chloromethanethioyl)dimethylamine

Molecular FormulaC3H6ClNS

InChI KeyPHWISQNXPLXQRU-UHFFFAOYSA-N

SMILESCN(C)C(Cl)=S

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規格

規格表

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.

RUO – Research Use Only

General References:

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.
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.