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Chemical Structure| 53218-26-1 Chemical Structure| 53218-26-1
Chemical Structure| 53218-26-1

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Product Details of 6-Bromobenzo[d]thiazole

CAS No. :53218-26-1
Formula : C7H4BrNS
M.W : 214.08
SMILES Code : BrC1=CC=C2N=CSC2=C1
MDL No. :MFCD04115372
InChI Key :YJOUISWKEOXIMC-UHFFFAOYSA-N
Pubchem ID :2795171

Safety of 6-Bromobenzo[d]thiazole

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of 6-Bromobenzo[d]thiazole

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 53218-26-1 ]

[ 53218-26-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 557-21-1 ]
  • [ 53218-26-1 ]
  • [ 58249-61-9 ]
  • 2
  • [ 53218-26-1 ]
  • [ 51618-30-5 ]
YieldReaction ConditionsOperation in experiment
75% With 1.3-propanedithiol; dimethyl sulfoxide; potassium hydroxide; at 130℃; for 12h;Inert atmosphere; General procedure: To a solution of benzothiazoles or benzoxazoles (1, 1 mmol) in DMSO (3 mL), was added KOH (280 mg, 5 equiv) and 1,3-propanedithiol (207 muL, 2 mmol). The reaction mixture was heated under argon at 130 C for 12 h. After cooling to room temperature, water (10 mL) was added. The pH of the reaction mixture was adjusted to 3-4 using 5% HCl. The resulting mixture was extracted with ethyl acetate (15 mL ×2). The organic layer was washed with water and brine, dried over anhydrous MgSO4 and concentrated using rotary evaporator. The crude product was purified by silica gel column chromatography using ethyl acetate/n-hexane as eluent to afford the corresponding heteroaryl thiols 3.
 

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