ChemicalBook--->CAS DataBase List--->3507-27-5

3507-27-5

3507-27-5 Structure

3507-27-5 Structure
IdentificationBack Directory
[Name]

Benzothiazole, 2-chloro-4-methoxy- (6CI,7CI,8CI,9CI)
[CAS]

3507-27-5
[Synonyms]

12944-A3
2-chloro-4-methoxybenzothiazle
Benzothiazole, 2-chloro-4-Methoxy-
2-chloro-4-methoxybenzo[d]thiazole
Benzothiazole, 2-chloro-4-methoxy- (6CI,7CI,8CI,9CI)
[Molecular Formula]

C8H6ClNOS
[MDL Number]

MFCD04448819
[MOL File]

3507-27-5.mol
[Molecular Weight]

199.66
Chemical PropertiesBack Directory
[Melting point ]

66 °C
[Boiling point ]

293.5±13.0 °C(Predicted)
[density ]

1.404±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-0.08±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C8H6ClNOS/c1-11-5-3-2-4-6-7(5)10-8(9)12-6/h2-4H,1H3
[InChIKey]

MCCTXJVKIFYBJV-UHFFFAOYSA-N
[SMILES]

S1C2=CC=CC(OC)=C2N=C1Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

29342000
Hazard InformationBack Directory
[Chemical Properties]

Pale yellow liquid
[Synthesis]

4-Methoxy-2-aminobenzothiazole

5464-79-9

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

3507-27-5

The general procedure for the synthesis of 2-chloro-4-methoxybenzo[d]thiazole using 2-amino-4-methoxybenzothiazole as starting material was as follows: copper(II) chloride (3.36 g, 25.0 mmol), acetonitrile (71 mL), and isoamyl nitrite (2.2 mL, 16.6 mmol) were added to a 500 mL three-neck flask equipped with a condenser under nitrogen protection. The suspension was placed in a 65 °C oil bath and stirred for 10 min, followed by the slow addition of a solution of 2-amino-4-methoxybenzothiazole (2.00 g, 11.1 mmol) in acetonitrile (42 mL). The reaction mixture was stirred continuously in an oil bath at 65 °C for 2 h and subsequently cooled to 20 °C. Water (150 mL) and 1N hydrochloric acid (100 mL) were added to the reaction mixture, followed by extraction with ethyl acetate (3 x 100 mL). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. The resulting residue was purified by silica gel column chromatography (5% to 15% gradient with ethyl acetate in hexane as eluent) to afford 2-chloro-4-methoxybenzo[d]thiazole (1.52 g, 69% yield) as a white solid.

[References]

[1] Patent: WO2016/197078, 2016, A1. Location in patent: Paragraph 626
[2] Gazzetta Chimica Italiana, 1964, vol. 94, p. 372 - 381
Spectrum DetailBack Directory
[Spectrum Detail]

Benzothiazole, 2-chloro-4-methoxy- (6CI,7CI,8CI,9CI)(3507-27-5)1HNMR
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