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7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one
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7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one

CAS: 129722-34-5

Ref. 3D-FB19204

10g
68.00 €
25g
120.00 €
50g
189.00 €
100g
325.00 €
250g
630.00 €
Estimated delivery in United States, on Tuesday 28 May 2024

Product Information

Name:
7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one
Synonyms:
  • 7-(4-Bromobutoxy)-3,4-dihydro-2(1H)-quinolinone
  • 2(1H)-Quinolinone, 7-(4-bromobutoxy)-3,4-dihydro-
  • 3,4-Dihydro-7-(4-Bromobutoxy)-2(1H)-Quinolinone
  • 3,4-Dihydro-7-(4-bromo butoxy)-2(1H)-quinolinone
  • 7-(3-bromopropoxy)-3,4-dihydro-1H-quinolin-2-one
  • 7-(4-Bromobutoxy)-1,2,3,4-tetrahydroquinoline-2-one
  • 7-(4-Bromobutoxy)-2(1H)-3,4-Dihydroquinolinone
  • 7-(4-Bromobutoxy)-3,4-Dihydro-2-Quinolinone
  • 7-(4-Bromobutoxy)-3,4-dihydroquinoline-2(1H)-one
  • 7-(4-Bromobutoxy)3,4-dihyrdro-2(H)-Quinolinone
  • See more synonyms
  • 7-(4-bromo-butoxy)-3,4-dihydro-1H-quinolin-2-one
  • 7-(4-bromobutoxy)-3,4-dihydroquinolin-2(1H)-one
  • 7-hydroxy-(4-Bromobutyloxy)-2(1H)-3,4-dihydroquinolinone
  • Lanzapine
Description:

7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one is a palladium catalyst that can be used in a Buchwald reaction. This reaction is an industrially scalable process that has been developed to produce high yields of valuable organic compounds from inexpensive starting materials. The catalytic cycle involves the formation of the palladium species Pd(0) followed by its oxidative addition to an alkyl halide. This addition leads to the formation of a palladium(II) species and subsequent reductive elimination of hydrogen halide. 7-(4-Bromobutoxy)-3,4-dihydroquinolin-2-one is used as a catalyst in this process because it selectively reacts with electron rich aromatic substrates to form substituted benzoquinones or phenols. The product distribution is determined by the reactivity of the substrate and the relative rates of competing reactions. Impurities are formed during synthesis due to

Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
298.18 g/mol
Formula:
C13H16BrNO2
Purity:
Min. 95%
InChI:
InChI=1S/C13H16BrNO2/c14-7-1-2-8-17-11-5-3-10-4-6-13(16)15-12(10)9-11/h3,5,9H,1-2,4,6-8H2,(H,15,16)
InChI key:
InChIKey=URHLNHVYMNBPEO-UHFFFAOYSA-N
SMILES:
O=C1CCc2ccc(OCCCCBr)cc2N1
MDL:
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EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
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Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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