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[ CAS No. 1520-21-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1520-21-4
Chemical Structure| 1520-21-4
Structure of 1520-21-4 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Jang, Mingyeong ; Lim, Taeho ; Park, Byoung Yong , et al. DOI: PubMed ID:

Abstract: In this study, we developed a metal-free and highly chemoselective method for the reduction of aromatic nitro compounds. This reduction was performed using tetrahydroxydiboron [B2(OH)4] as the reductant and 4,4'-bipyridine as the organocatalyst and could be completed within 5 min at room temperature. Under optimal conditions, nitroarenes with sensitive functional groups, such as vinyl, ethynyl, carbonyl, and halogen, were converted into the corresponding anilines with excellent selectivity while avoiding the undesirable reduction of the sensitive functional groups.

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Product Details of [ 1520-21-4 ]

CAS No. :1520-21-4 MDL No. :MFCD00015329
Formula : C8H9N Boiling Point : -
Linear Structure Formula :C6H4(CHCH2)(NH2) InChI Key :LBSXSAXOLABXMF-UHFFFAOYSA-N
M.W : 119.16 Pubchem ID :73700
Synonyms :

Safety of [ 1520-21-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1520-21-4 ]

* 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 [ 1520-21-4 ]

[ 1520-21-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1520-21-4 ]
  • [ 86688-96-2 ]
  • [ 134226-28-1 ]
  • 2
  • [ 3939-23-9 ]
  • [ 1520-21-4 ]
  • [ 1256379-25-5 ]
  • 3
  • [ 1520-21-4 ]
  • [ 2365-48-2 ]
  • [ 20637-09-6 ]
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