| Identification | More | [Name]
2-Chloro-5-chloromethylthiazole | [CAS]
105827-91-6 | [Synonyms]
2-CHLORO-5-CHLOROMETHYL-1,3-THIAZOLE
2-CHLORO-5-CHLOROMETHYLTHIAZOLE
2-chloro-5-(chloromethyl)thiozole
Thiazole, 2-chloro-5-(chloromethyl)-(9CI)
2-Chloro-5-(chlormethyl)thiazole
2-Chloro-5-chloromehtylthiazole
2-Chloro-5-Chloromethyl
ccmt
2-CHLORO-5-(CHLOROMETHYL)-1,3-THIAZOLE[FOR THIAMETHOXAM]
2-CHLORO-5-CHLOROMETHYL THIAZOLE, 98+% | [EINECS(EC#)]
429-830-5 | [Molecular Formula]
C4H3Cl2NS | [MDL Number]
MFCD01073549 | [Molecular Weight]
168.04 | [MOL File]
105827-91-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
31 | [Boiling point ]
268.6±32.0 °C(Predicted) | [density ]
1.503±0.06 g/cm3(Predicted) | [refractive index ]
n20/D1.571 | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [solubility ]
soluble in Methanol | [form ]
neat | [pka]
0.19±0.10(Predicted) | [color ]
White to Light yellow | [BRN ]
5861439 | [InChI]
InChI=1S/C4H3Cl2NS/c5-1-3-2-7-4(6)8-3/h2H,1H2 | [InChIKey]
VRMUIVKEHJSADG-UHFFFAOYSA-N | [SMILES]
S1C(CCl)=CN=C1Cl | [CAS DataBase Reference]
105827-91-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37:Wear suitable gloves . | [RIDADR ]
2922 | [WGK Germany ]
3 | [Hazard Note ]
Irritant | [HazardClass ]
8 | [PackingGroup ]
Ⅱ | [HS Code ]
29349990 |
| Questions And Answer | Back Directory | [Description]
2-Chloro-5-chloromethylthiazole is used as pharmaceutical and agrochemical intermediate. It is also used as intermediate of insecticides Thiamethoxam and Clothianidin. It is also useful in in the synthesis of Ritonavir (R535000); a second-generation anti-AIDS drug and a selective HIV protease inhibitor.
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| Hazard Information | Back Directory | [Chemical Properties]
White crystal or powder | [Uses]
2-Chloro-5-(chloromethyl)thiazole is a useful synthetic intermediate used in the synthesis of Ritonavir (R535000) | [Synthesis]
To a 2-liter round bottomed flask equipped with a mechanical stirrer, thermometer and a condenser, whose outlet was vented into an aqueous sodium hydroxide trap, was charged the crude mixture of cis- and trans-3-chloropropenyl isothiocyanates (504.2 g, 3.79 mol) and chloroform (600 mL). The mixture was stirred and heated to reflux. Chlorine (267.1 g, 3.77 mole) gas was bubbled under the surface of the reaction over a period of 6-8 h. The conversion of the isothiocyanates to 2-chloro-5- (chloromethyl)thiazole was monitored by GC. When the reaction was shown to be complete by GC analysis, the reaction mixture was cooled and then filtered. The filtrate was concentrated on the rotary evaporator to remove chloroform. Sodium bicarbonate (approximately 0.25 equivalents) was added to the concentrated filtrate, and the product 2-chloro-5-chloromethylthiazole was distilled at 97 °C under vacuum (6mm/Hg). The yield after distillation was 43%. 1 H NMR (CDCl3) δ: 7.3 (s, 1H); 4.6 (s, 2H). 13C NMR (CDCl3) δ: 152.6 (C-2); 140.2 (C-4); 137.5 (C-5); 37.1 (-CH2-).
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