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| CAS No.: | 6142-15-0 |
|---|---|
| Name: | 2-AMINO-4-METHYLTHIAZOLE HYDROCHLORIDE |
| Article Data: | 1 |
| Molecular Structure: | |
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| Formula: | C4H7ClN2S |
| Molecular Weight: | 150.632 |
| Synonyms: | 2-Thiazolamine,4-methyl-, monohydrochloride (9CI);Thiazole, 2-amino-4-methyl-, hydrochloride(7CI);Thiazole, 2-amino-4-methyl-, monohydrochloride (8CI);2-Amino-4-methylthiazole hydrochloride;4-Methyl-2-thiazolaminemonohydrochloride; |
| Melting Point: | 173 °C |
| Boiling Point: | 232.5 °C at 760 mmHg |
| Flash Point: | 94.4 °C |
| Solubility: | almost transparency |
| PSA: | 67.15000 |
| LogP: | 2.41690 |
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Specification
The 2-Thiazolamine,4-methyl-, hydrochloride is an organic compound with the formula C4H7ClN2S. The systematic name of this chemical is 4-Methyl-1,3-thiazol-2-amine hydrochloride. With the CAS registry number 6142-15-0, it is also named as 2-Amino-4-methylthiazole Hydrochloride. Besides, its molecular weight is 150.63.
The physical properties of 2-Thiazolamine,4-methyl-, hydrochloride are: (1)ACD/LogP: 0.84; (2)ACD/LogD (pH 7.4): 0.81; (3)ACD/BCF (pH 5.5): 1; (4)ACD/BCF (pH 7.4): 2.38; (5)ACD/KOC (pH 5.5): 9.9; (6)ACD/KOC (pH 7.4): 63.44; (7)#H bond acceptors: 2; (8)#H bond donors: 2; (9)Polar Surface Area: 44.37 Å2; (10)Flash Point: 94.4 °C; (11)Enthalpy of Vaporization: 46.92 kJ/mol; (12)Boiling Point: 232.5 °C at 760 mmHg; (13)Vapour Pressure: 0.0588 mmHg at 25 °C.
Uses of 2-Thiazolamine,4-methyl-, hydrochloride: it can be used to produce 6-(4-Methyl-2-thiazolyl)-3-methylthiazolo[3,2-a]-1,3,5-triazine-5,7-dithione and 2-Isothiocyanato-4-methyl-thiazole. It will need reagent calcium carbonate and solvents H2O and benzene with reaction time of 3 hours. The yield is about 36%.
![2-Thiazolamine,4-methyl-, hydrochloride and Thiocarbonyl dichloride can be used to produce 6-(4-Methyl-2-thiazolyl)-3-methylthiazolo[3,2-a]-1,3,5-triazine-5,7-dithione and 2-Isothiocyanato-4-methyl-thiazole](/UserFilesUpload/Uses of 2-Thiazolamine,4-methyl-, hydrochloride 1.png)
![2-Thiazolamine,4-methyl-, hydrochloride and Thiocarbonyl dichloride can be used to produce 6-(4-Methyl-2-thiazolyl)-3-methylthiazolo[3,2-a]-1,3,5-triazine-5,7-dithione and 2-Isothiocyanato-4-methyl-thiazole](/UserFilesUpload/Uses of 2-Thiazolamine,4-methyl-, hydrochloride 2.png)
![2-Thiazolamine,4-methyl-, hydrochloride and Thiocarbonyl dichloride can be used to produce 6-(4-Methyl-2-thiazolyl)-3-methylthiazolo[3,2-a]-1,3,5-triazine-5,7-dithione and 2-Isothiocyanato-4-methyl-thiazole](/UserFilesUpload/Uses of 2-Thiazolamine,4-methyl-, hydrochloride 3.png)
You can still convert the following datas into molecular structure:
(1)SMILES: Cl.n1c(csc1N)C
(2)InChI: InChI=1/C4H6N2S.ClH/c1-3-2-7-4(5)6-3;/h2H,1H3,(H2,5,6);1H
(3)InChIKey: WUMMJVLSXMYDRW-UHFFFAOYAF
(4)Std. InChI: InChI=1S/C4H6N2S.ClH/c1-3-2-7-4(5)6-3;/h2H,1H3,(H2,5,6);1H
(5)Std. InChIKey: WUMMJVLSXMYDRW-UHFFFAOYSA-N