2-Chloro-5-chloromethylthiazole CAS 105827-91-6

Introduction:Basic information about 2-Chloro-5-chloromethylthiazole CAS 105827-91-6, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2-Chloro-5-chloromethylthiazole Basic informationDescription

Product Name:2-Chloro-5-chloromethylthiazole
Synonyms:2-CHLORO-5-CHLOROMETHYLTHIAZOLE;2-CHLORO-5-CHLOROMETHYL-1,3-THIAZOLE;2-CHLORO-5-(CHLOROMETHYL)-1,3-THIAZOLE[FOR THIAMETHOXAM];2-CHLORO-5-CHLOROMETHYL THIAZOLE, 98+%;2-chloro-5-(chloromethyl)thiozole;Thiazole, 2-chloro-5-(chloromethyl)- (9CI);2-Chloro-5-(chlormethyl)thiazole;2-Chloro-5-chloromehtylthiazole
CAS:105827-91-6
MF:C4H3Cl2NS
MW:168.04
EINECS:429-830-5
Product Categories:Thiazoles;Pesticide intermediate;HALOMETYL;Miscellaneous;API;bc0001;105827-91-6
Mol File:105827-91-6.mol

2-Chloro-5-chloromethylthiazole Chemical Properties

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
pka0.19±0.10(Predicted)
color White to Light yellow
BRN 5861439
InChIInChI=1S/C4H3Cl2NS/c5-1-3-2-7-4(6)8-3/h2H,1H2
InChIKeyVRMUIVKEHJSADG-UHFFFAOYSA-N
SMILESS1C(CCl)=CN=C1Cl
CAS DataBase Reference105827-91-6(CAS DataBase Reference)

Safety Information

Hazard Codes Xi,N,T
Risk Statements 36/37/38-51/53-43-34-24-22
Safety Statements 26-37-61-45-36/37/39
RIDADR 2922
WGK Germany 3
Hazard Note Irritant
HazardClass 8
PackingGroup 
HS Code 29349990

2-Chloro-5-chloromethylthiazole Usage And Synthesis

Description2-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.
Chemical PropertiesWhite crystal or powder
Uses2-Chloro-5-(chloromethyl)thiazole is a useful synthetic intermediate used in the synthesis of Ritonavir (R535000)
SynthesisTo 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-).
References[1] Patent: CN108484524, 2018, A. Location in patent: Paragraph 0051; 0052; 0053; 0054
[2] Patent: CN105294595, 2016, A. Location in patent: Paragraph 0013; 0014; 0015; 0016; 0017
[3] Journal of Agricultural and Food Chemistry, 2004, vol. 52, # 7, p. 1918 - 1922
[4] Patent: CN107935960, 2018, A. Location in patent: Paragraph 0031-0043
[5] Patent: CN105949145, 2016, A. Location in patent: Paragraph 0045; 0046

2-Chloro-5-chloromethylthiazole Preparation Products And Raw materials

Raw materialsChloroform-->Sulfuryl chloride-->2-chloro-3-isothiocyanato-prop-1-ene-->2-Chloro-5-methylthiazole-->Lenalidomide Impurity 13-->5-METHYLENE-1,3-THIAZOLIDINE-2-THIONE-->1-Propene, 3-chloro-1-isothiocyanato-, (1E)--->Allyl isothiocyanate-->Chlorine-->Carbon tetrachloride
Preparation Products2-[(2-Chloro-thiazol-5-ylMethyl)-aMino]-ethanol-->Thiamethoxam
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