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Chemical Structure| 693-92-5 Chemical Structure| 693-92-5

Structure of 693-92-5

Chemical Structure| 693-92-5

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Product Details of [ 693-92-5 ]

CAS No. :693-92-5
Formula : C4H5NS
M.W : 99.15
SMILES Code : CC1=NSC=C1
MDL No. :MFCD00955579

Safety of [ 693-92-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 693-92-5 ]

* 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 [ 693-92-5 ]

[ 693-92-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 693-92-5 ]
  • [ 4576-90-3 ]
YieldReaction ConditionsOperation in experiment
23% With chromium(VI) oxide; sulfuric acid; at 0 - 20℃; for 16h;Inert atmosphere; To a stirred solution of compound 39 (10 g, 100.85 mmol) in concentrated sulfuric acid (300 mL) under inert atmosphere was added chromium (VI) oxide (30.25 g, 302.57 mmol) portion wise at 0 oC, followed by warming to room temperature and stirring for 16 h. The reaction was monitored by TLC. After completion of the reaction, the reaction mixture was quenched with ice-cold water (3 L) slowly and extracted with diethyl ether (10 x 600 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to afford crude compound 40 (3 g, 23%) as white solid. TLC: 20% EtOAc/ hexanes (Rf: 0.1).1H-NMR (DMSO-d6, 400 MHz): delta 10.95 (br.s, 1H), 9.16 (d, J = 4.6 Hz, 1H), 7.80 (d, J = 4.6 Hz, 1H); LCMS Calculated for C4H3NO2S: 128.99; Observed: 130.4 (M+1)+.
13% With sulfuric acid; sulfur trioxide; chromium(VI) oxide; at 0 - 20℃; for 16h; Chromium(IV) oxide (9.00 mmol) is added in several batches to a solution of 3-methylisothiazole (3.03 mmol) in fuming sulfuric acid (10 ml_) at 0 0C. The reaction mixture is allowed to warm to rt and is maintained for 16 h. The reaction mixture is diluted with ice water (100 ml_), extracted with ether (6 x 200 ml_) and the combined organic layers are dried (sodium sulfate) and concentrated. The residue is purified by preparative HPLC to provide isothiazole-3-carboxylic acid in 13% yield as a white solid. 1H-NMR (400MHz, DMSO-Cf6) 5 3.43 (s, 1 H), 9.17 (d, 1 H), 7.80 (d, 1 H), 3.43 (s, 1 H); LC/MS (ES, m/z) [M+I]+ 128.
 

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