Carbamothioic chloride, dimethyl-

• Formula: C₃H₆ClNS
• Molecular weight: 123.604
• IUPAC Standard InChI: InChI=1S/C3H6ClNS/c1-5(2)3(4)6/h1-2H3 Copy

  
• IUPAC Standard InChIKey: PHWISQNXPLXQRU-UHFFFAOYSA-N Copy
• CAS Registry Number: 16420-13-6
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Carbamoyl chloride, dimethylthio-; Dimethylthiocarbamoyl chloride; Dimethylthiocarbamyl chloride; N,N-Dimethylthiocarbamoyl chloride; N,N-Dimethylthiocarbamyl chloride
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Mass spectrum (electron ionization)
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Normal melting point

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Pudovik, Khairullin, et al., 1989
Pudovik, A.N.; Khairullin, V.K.; Vasyanina, M.A.; Kamalov, R.M.; Kataeva, O.N.; Litvinov, I.A.; Naumov, V.A., Synthesis and Structure of the Dimethylamide of Chloroformic Acid and Its Reaction with Potassium Thiocyanate, Izv. Akad. Nauk SSSR, Ser. Khim., 1989, 38, 909-13. [all data]

Jen and Cava, 1983
Jen, K.-Y.; Cava, M.P., J. Org. Chem., 1983, 48, 1449-51. [all data]

Kristian, Koscik, et al., 1973
Kristian, P.; Koscik, D.; Bernat, J., Isothiocyanates and Tynthetic Producers XIII. Preparation and Spectral Properties of 2,,6-Trisubstituted 5,6-Dihydro-4H-1,3,5-thiadiazine-4- thiones, Chem. Zvesti, 1973, 27, 280-5. [all data]

Walter and Becker, 1972
Walter, W.; Becker, R.F., Justus Liebigs Ann. Chem., 1972, 755, 145-72. [all data]

Goerdeler and Luedke, 1970
Goerdeler, J.; Luedke, H., Chem. Ber., 1970, 103, 3393-3406. [all data]

Newman and Hetzel, 1969
Newman, M.S.; Hetzel, F.W., J. Org. Chem., 1969, 34, 3604-6. [all data]

Birkofer and Krebs, 1968
Birkofer, L.; Krebs, K., Organosilicon Compou9nds XXXV. N,N-Disubstituted Carbonyl and Thiocarbamoyl Chlorides via Silyl Derivatives, Tetrahedron Lett., 1968, 885-8. [all data]

Hasserodt, 1968
Hasserodt, U., Chem. Ber., 1968, 101, 113-20. [all data]

Neuman, Roark, et al., 1967
Neuman, R.C.; Roark, D.N.; Jonas, V., Studies of Chemical Excange by Nuclear Magnetic Resonance II. Hindered Rotation in Amides and Thioamides, J. Am. Chem. Soc., 1967, 89, 3412-6. [all data]

Lieber, Rao, et al., 1963
Lieber, E.; Rao, C.N.R.; Layer, C.B.; Trivedi, J.P., 5-Disubstituted)amino-1,2,3,4-thiatriazoles, Can. J. Chem., 1963, 41, 1643-4. [all data]

Lieber and Trivedi, 1960
Lieber, E.; Trivedi, J.P., Thiphosgenation of Dimethylammonium Chloride, J. Org. Chem., 1960, 25, 650-1. [all data]

Goshorn, Levis, et al., 1955
Goshorn, R.H.; Levis, W.W., Jr.; Jaul, E.; Ritter, E.J., Diethylcarbamyl Chloride, Org. Synthesis, 1955, 35, 55-8. [all data]

Billeter, 1893
Billeter, O., Chem. Ber., 1893, 26, 1686. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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