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Chemical Structure| 6007-90-5 Chemical Structure| 6007-90-5

Structure of 6007-90-5

Chemical Structure| 6007-90-5

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Product Details of [ 6007-90-5 ]

CAS No. :6007-90-5
Formula : C7H11NS
M.W : 141.23
SMILES Code : NCCCC1=CC=CS1
MDL No. :MFCD09886636
InChI Key :CUGBKQGQESIBMN-UHFFFAOYSA-N
Pubchem ID :40835

Safety of [ 6007-90-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 6007-90-5 ]

* 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 [ 6007-90-5 ]

[ 6007-90-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6007-90-5 ]
  • [ 161622-05-5 ]
  • 3-fluoro-5-(trifluoromethyl)-N-(3-(thiophen-2-yl)propyl)benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With benzotriazol-1-ol; diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 20℃; General procedure: To asolution of aminoalkylthiophene or bisaminoalkylthiophene inDMF (10 mL), 1 equivalent of I'-diisopropylcarbodiimide (DIC),hydroxybenzotriazole (HOBT), and <strong>[161622-05-5]3-fluoro-5-(trifluoromethyl)benzoic acid</strong> (1 mmol amino group for one equivalent) was addedand stirred 12 h. The solution was then evaporated under reducedpressure. The crude was purified with column chromatography(silica gel 100-200 mesh), using hexane/DCM as eluent to yield F4-Thiophene derivatives (1sa, 1sd, 1se, 2se, 2sf, 3sm, 3sl) and F4-Thiophene-F4 derivatives (1sf, 2sh, 2si, 2sj, 2sg, 3sn, 3so) as finalproducts. Yield 60%-70%.
With benzotriazol-1-ol; diisopropyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide; at 20℃; for 12h; In a round bottom flask, 5 mL of DMF, 5 mLDCM,1 mmol of 2-propylaminothiophene,1 mmol DIC, 1 mmol HOBTAnd 1 mmol of <strong>[161622-05-5]3-fluoro-5-trifluoromethylbenzoic acid</strong>.The reaction was stirred at room temperature for 12 hours.The solvent was then removed by distillation under reduced pressure and purified by column chromatography to give the product as a pale yellow solid 3-fluoro-5- (trifluoromethyl) -N- (3- (2-thienyl) propyl) benzamide(3-fluoro-5- (trifluoromethyl) -N- (3- (thiophen-2-yl) propyl) benzamide Compound No. 1sd).
 

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