Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI)

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Products Intro: Product Name:2,4-Dimethylbenzothiazole
CAS:5262-63-5
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:2,4-Dimethylbenzo[d]thiazole
CAS:5262-63-5
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-62319
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CAS:5262-63-5
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Products Intro: Product Name: Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI)
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Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI) manufacturers

Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI) Basic information
Product Name:Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI)
Synonyms:Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI);2,4-Dimethylbenzothiazole;2,4-DiMethylbenzo[d]thiazole;2,4-Dimethyl-benzthiazol;2,4-dimethyl-1,3-benzothiazole;Benzothiazole, 2,4-dimethyl-
CAS:5262-63-5
MF:C9H9NS
MW:163.24
EINECS:
Product Categories:BENZOTHIAZOLE
Mol File:5262-63-5.mol
Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI) Structure
Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI) Chemical Properties
Melting point 33-34 °C
Boiling point 128-130 °C(Press: 20 Torr)
density 1.176±0.06 g/cm3(Predicted)
pka2.19±0.10(Predicted)
Safety Information
MSDS Information
Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI) Usage And Synthesis
Chemical PropertiesWhite solid
Uses2,4-Dimethyl-benzothiazole, is used in the preparation of quaternary salts of chalcogenites as photographic sensitizers.
Synthesis
NSC402535

35274-15-8

Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI)

5262-63-5

[Step 2] Potassium hexacyanoferrate(III) (22.1 g) was mixed with water (35 mL), and a mixture of N-(2-methylphenyl)ethylthioamide (6.60 g), sodium hydroxide (3.69 g), and water (50 mL) made in Step 1 was added. The reaction system was stirred at 40°C for 2 hours. After completion of the reaction, it was cooled to room temperature and extracted twice with ethyl acetate (50 mL). The organic phases were combined, washed with saturated saline (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford 2,4-dimethylbenzothiazole (Compound 13) (2.82 g). The 1H-NMR (CDCl3) data of compound 13 were as follows: δ 7.66 (m, 1H), 7.24 (m, 2H), 2.85 (s, 3H), 2.73 (s, 3H).

References[1] Bulletin de la Societe Chimique de France, 1956, p. 684,688
[2] Zhurnal Obshchei Khimii, 1957, vol. 27, p. 3097,3103, 1305;engl. Ausg. S. 3138, 3143, 3144
[3] Yakugaku Zasshi, 1950, vol. 70, p. 540
[4] Chem.Abstr., 1951, p. 7111
[5] Patent: WO2015/194676, 2015, A1. Location in patent: Paragraph 0034
Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI) Preparation Products And Raw materials
Raw materialsNSC402535
Tag:Benzothiazole, 2,4-dimethyl- (6CI,7CI,8CI,9CI)(5262-63-5) Related Product Information
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