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Chemical Structure| 615-55-4 Chemical Structure| 615-55-4

Structure of 615-55-4

Chemical Structure| 615-55-4

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CAS No.: 615-55-4

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Product Details of [ 615-55-4 ]

CAS No. :615-55-4
Formula : C6H5Br2N
M.W : 250.92
SMILES Code : NC1=CC=C(Br)C(Br)=C1
MDL No. :MFCD00041310
Boiling Point : No data available
InChI Key :QFTJOYLPELHHCO-UHFFFAOYSA-N
Pubchem ID :521981

Safety of [ 615-55-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P280

Application In Synthesis of [ 615-55-4 ]

* 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 [ 615-55-4 ]

[ 615-55-4 ] Synthesis Path-Downstream   1~33

  • 1
  • [ 75-15-0 ]
  • [ 615-55-4 ]
  • [ 119043-66-2 ]
  • 2
  • [ 504-66-5 ]
  • [ 615-55-4 ]
  • <i>N</i>-cyano-<i>N</i>'-(3,4-dibromo-phenyl)-guanidine [ No CAS ]
  • 3
  • [ 5411-50-7 ]
  • [ 615-55-4 ]
  • 6
  • [ 615-55-4 ]
  • [ 60956-24-3 ]
  • 9
  • 3-bromo-<i>N</i>-(2,3-dibromo-3-phenyl-propyliden)-aniline [ No CAS ]
  • [ 615-55-4 ]
  • 10
  • [ 615-55-4 ]
  • [ 127099-85-8 ]
  • 1-(3,4-dibromo-phenyl)-biguanide [ No CAS ]
  • 11
  • [ 615-55-4 ]
  • [ 77-78-1 ]
  • [ 60469-89-8 ]
  • 12
  • [ 615-55-4 ]
  • [ 77-78-1 ]
  • 3,4-dibromo-tri-<i>N</i>-methyl-anilinium; tribromoide [ No CAS ]
  • 13
  • [ 591-19-5 ]
  • [ 615-55-4 ]
YieldReaction ConditionsOperation in experiment
78% With tetrabutylammomium bromide; copper(ll) bromide; In ethanol; at 25℃; General procedure: A round bottom flask was charged with Bu4NBr (2 mmol, 0.64 g), EtOH (8 mL) and 2-methylaniline (2 mmol, 0.21 g) followed by CuBr2 (3 mmol, 0.67 g). The resulted mixture was stirred at 25 C. After the completion of the reaction (monitored by TLC), the solvent was evaporated under reduced pressure. To the residue was added ammonium hydroxide (5 mL, 25% w/v) and water (5 mL) with stirring, and the suspension was extracted with DCM(10 mL×4) The organic phase was washed with saturated brine and dried over anhydrous Na2SO4. The product 2b was obtained using flash chromatograph column eluted with PE : EA (5 : 1).
  • 15
  • [ 59-49-4 ]
  • [ 50-00-0 ]
  • [ 615-55-4 ]
  • 3-(3,4-dibromo-anilinomethyl)-3<i>H</i>-benzooxazol-2-one [ No CAS ]
  • 16
  • [ 615-55-4 ]
  • [ 87014-71-9 ]
  • [ 123-62-6 ]
  • [ 67450-65-1 ]
  • 17
  • [ 615-55-4 ]
  • [ 1548-13-6 ]
  • [ 23747-86-6 ]
  • 18
  • [ 628-71-7 ]
  • [ 615-55-4 ]
  • [ 121866-24-8 ]
  • 19
  • [ 615-55-4 ]
  • [ 87781-93-9 ]
  • [ 123994-76-3 ]
  • 20
  • [ 615-55-4 ]
  • [ 140-89-6 ]
  • [ 126190-11-2 ]
  • 21
  • [ 615-55-4 ]
  • (±)-trans-2-(dimethylamino)cyclopentyl methanesulfonate [ No CAS ]
  • (1S,2S)-N-(3,4-Dibromo-phenyl)-N',N'-dimethyl-cyclopentane-1,2-diamine [ No CAS ]
  • 22
  • [ 608-22-0 ]
  • [ 823-54-1 ]
  • [ 615-55-4 ]
  • [ 642-95-5 ]
  • 2,3-dibromo-4-chloroaniline [ No CAS ]
  • [ 591-19-5 ]
  • 23
  • [ 615-55-4 ]
  • [ 703-59-3 ]
  • [ 137840-21-2 ]
  • 24
  • [ 615-55-4 ]
  • [ 75-36-5 ]
  • [ 24108-97-2 ]
  • 27
  • [ 591-19-5 ]
  • [ 823-54-1 ]
  • [ 615-55-4 ]
  • [ 608-22-0 ]
  • 29
  • [ 615-55-4 ]
  • [ 407-25-0 ]
  • [ 179061-90-6 ]
  • 30
  • [ 615-55-4 ]
  • [ 71-43-2 ]
  • [ 60108-72-7 ]
  • 31
  • [ 615-54-3 ]
  • [ 7664-41-7 ]
  • sodium amide [ No CAS ]
  • [ 626-39-1 ]
  • [ 615-55-4 ]
YieldReaction ConditionsOperation in experiment
Following the procedure of Example 3 the following substituted anilines: 3,4-dibromoaniline 3,4-difluoroaniline 3-chloro-4-bromoaniline
 

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