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Methomyl

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Identification
Molecular formula
C5H10N2OS2
CAS number
16752-77-5
IUPAC name
3,5-dimethyl-1,3,5-thiadiazinane-2-thione
State
State

At room temperature, Methomyl exists as a crystalline solid. It is stable under normal temperatures and pressures.

Melting point (Celsius)
78.50
Melting point (Kelvin)
351.65
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
162.27g/mol
Molar mass
162.2440g/mol
Density
1.2940g/cm3
Appearence

Methomyl is a white, crystalline solid with no distinctive odor. It is typically available in solid form and can appear as granules or powder.

Comment on solubility

Solubility of 3,5-dimethyl-1,3,5-thiadiazinane-2-thione

The solubility of 3,5-dimethyl-1,3,5-thiadiazinane-2-thione can be influenced by various factors, including temperature and solvent type. Here are some key points to consider:

  • Polar vs. Nonpolar Solvents: This compound tends to dissolve better in polar solvents due to its functional groups, which can engage in hydrogen bonding and dipole interactions.
  • Temperature Dependence: Increasing temperature usually enhances solubility, as the kinetic energy of the molecules increases, leading to more effective interactions with the solvent.
  • Hydrogen Bonding Capability: The presence of nitrogen and sulfur in the compound allows it to form hydrogen bonds, which can aid solubility in suitable environments.
  • Structural Considerations: The branched structure, as indicated by "dimethyl," can affect how molecules stack or pack, thus influencing solubility characteristics.

To summarize, while the solubility of 3,5-dimethyl-1,3,5-thiadiazinane-2-thione in water is limited, it may show better solubility in polar organic solvents. Understanding these solubility dynamics is crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 3,5-Dimethyl-1,3,5-thiadiazinane-2-thione

3,5-Dimethyl-1,3,5-thiadiazinane-2-thione is a fascinating compound with several unique properties and applications in the field of chemistry. Here are some interesting insights:

  • Thiadiazine Structure: This compound features a thiadiazinane ring structure, which is notable for its sulfur-containing framework. This can impart distinct chemical reactivity and stability compared to its oxygen analogs.
  • Key Functional Group: The presence of a thione group contributes to its reactivity, making it a potential candidate for various chemical transformations.
  • Synthesis: The synthesis of thiadiazine rings often involves the use of serious reagents and precise conditions. Understanding these methods can enhance a chemist's ability to create compounds with similar structures.
  • Biological Interest: Many thiadiazines are studied for their biological activity. They have shown potential in medicinal chemistry, as certain derivatives can exhibit antimicrobial or anti-inflammatory properties.
  • Practical Applications: Compounds related to thiadiazinanes find utility in agricultural and chemical industries, such as in the development of herbicides or pesticides.
  • Research Potential: With ongoing scientific research, the efficacy and applicability of 3,5-dimethyl-1,3,5-thiadiazinane-2-thione may lead to exciting discoveries in molecular medicine and green chemistry.

In summary, 3,5-dimethyl-1,3,5-thiadiazinane-2-thione stands out due to its unique structure and diverse applications in chemical research. Its exploration continues to be a valuable area of study for chemists interested in both synthetic and applied sciences.

Synonyms
DAZOMET
533-74-4
Basamid
3,5-Dimethyl-1,3,5-thiadiazinane-2-thione
Tiazon
Thiazone
Mylone
Carbothialdin
Dimethylformocarbothialdine
Prezervit
Nefusan
Thiazon
Crag nemacide
Basamid-Puder
Mico-fume
Basamid G
Basamid P
Crag 974
Basamide
Mylon
Mylone 85
Basamid-Granular
Fennosan B 100
Stauffer N 521
Crag fungicide 974
Nalcon 243
Thiadiazin (pesticide)
Crag 85W
UCC 974
Troysan 142
Dazomet-Powder BASF
3,5-Dimethyltetrahydro-1,3,5-thiadiazine-2-thione
Mylon [Czech]
Salvo [Czech]
2H-1,3,5-Thiadiazine-2-thione, tetrahydro-3,5-dimethyl-
Caswell No. 840
Dazomet [BSI:ISO]
NSC 4737
Dazomet [ISO]
2-Thio-3,5-dimethyltetrahydro-1,3,5-thiadiazine
N 521
Dazoberg
Micofume
HSDB 1642
Tetrahydro-3,5-dimethyl-2H-1,3,5-thiadiazine-2-thione
3,5-Dimethyl-2-thionotetrahydro-1,3,5-thiadiazine
EINECS 208-576-7
3,5-Dimethyltetrahydro-1,3,5-2H-thiadiazine-2-thione
3,5-Dimethyltetrahydro-2H-1,3,5-thiadiazine-2-thione
Tetrahydro-2H-3,5-dimethyl-1,3,5-thiadiazine-2-thione
EPA Pesticide Chemical Code 035602
UNII-S7419CG4W5
BRN 0116039
3,5-Dimethyl-1,2,3,5-tetrahydro-1,3,5-thiadiazinethione-2
DTXSID7024902
CHEBI:75212
S7419CG4W5
3,5-Dimethyl-1,3,5-(2H)-tetrahydrothiadiazine-2-thione
DAZOMET [HSDB]
NSC-4737
DAZOMET [MI]
3,5-Dimetil-peridro-1,3,5-tiadiazin-2-tione
3,5-Dimethylperhydro-1,3,5-thiadiazin-2-thion
Amerstat 233 (Salt/Mix)
3,5-Dimetil-peridro-1,3,5-tiadiazin-2-tione [Italian]
DTXCID004902
3,5-Dimethylperhydro-1,3,5-thiadiazin-2-thion [Czech, German]
4-27-00-07436 (Beilstein Handbook Reference)
THIADIAZIN [PESTICIDE]
3,5-Dimethyl-tetrahydro-1,3,5-thiadiazine-2-thione
3,5-Dimethyl-1,3,5-2H-tetrahydrothiadiazine-2-thione
3,5-Dimethyltetrahydro-1,3,5-2H-thioadiazine-2-thione
Tetrahydro-3,5-dimethyl-2H-1,3,5-thiodiazin-2-thione
3,5-Dimethyl tetrahydro-2-H,1,3,5-thiadiazone-2-thione
BasamidGranular
BasamidPuder
Basamid Purder
Basamid-Purder
Basimid G
DazometPowder BASF
2-Thio-3,5-dimethyl-tetrahydro-1,3,5-thiadiazine
BUSAN 1058
NALCO 5787
3,5Dimethyl1,3,5thiadiazinane2thione
3,5Dimetilperidro1,3,5tiadiazin2tione
USEPA/OPP Pesticide Code: 035602
3,5Dimethylperhydro1,3,5thiadiazin2thion
2Thio3,5dimethyltetrahydro1,3,5thiadiazine
3,5Dimethyl2thionotetrahydro1,3,5thiadiazine
3,5Dimethyltetrahydro1,3,5thiadiazine2thione
3,5Dimethyltetrahydro1,3,52Hthiadiazine2thione
3,5Dimethyltetrahydro2H1,3,5thiadiazine2thione
Tetrahydro2H3,5dimethyl1,3,5thiadiazine2thione
Tetrahydro3,5dimethyl2H1,3,5thiadiazine2thione
3,5Dimethyl1,2,3,5tetrahydro1,3,5thiadiazinethione2
208-576-7
carbothialdine
qayiciqnsgetas-uhfffaoysa-n
salvo
un2588
DMTT
D 35
NSC4737
Basamid - Purder
CAS-533-74-4
3,3,5-thiadiazine
Maybridge1_000020
MixCom1_000020
3,3,5-tiadiazin-2-tione
SCHEMBL21382
3,3,5-thiadiazin-2-thion
2-Thio-3,3,5-thiadiazine
MLS000104430
3,3,5-thiadiazine-2-thione
CHEMBL1407826
Dazomet Solution in Acetonitrile
3,3,5-2H-thiadiazine-2-thione
GLXC-02296
HMS2277P17
ML064
3,3,5-2H-thioadiazine-2-thione
CCG-2038
Tox21_201236
Tox21_300990
MFCD00023809
WLN: T6NYS ENTJ A1 BUS E1
AKOS006230484
Tetrahydro-3,3,5-thiadiazine-2-thione
NCGC00080412-01
NCGC00080412-02
NCGC00080412-03
NCGC00080412-04
NCGC00254892-01
NCGC00258788-01
AC-12680
AS-15262
SMR000054365
3,3,5-2H-tetrahydrothiadiazine-2-thione
Dazomet, PESTANAL(R), analytical standard
DB-052323
Tetrahydro-2H-3,3,5-thiadiazine-2-thione
MLS000104430-02
NS00006011
C18457
3,2,3,5-tetrahydro-1,3,5-thiadiazinethione-2
3,5-Dimethyl-1,3,5-thiadiazinane-2-thione #
Q424814
SR-01000641863-1
2H-1,5-Thiadiazine-2-thione, tetrahydro-3,5-dimethyl-
2H-1,3,5-Thiadiazine-2-thione, tetrahydro-3,5-dimethyl