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Merck
CN

653683

5-硝基吲哚-2-酮

97%

别名:

5-硝基-1,3-二氢-2H-吲哚-2-酮

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关于此项目

经验公式（希尔记法）:
C8H6N2O3
化学文摘社编号:
20870-79-5
分子量:
178.14
NACRES:
NA.22
PubChem Substance ID:
24883978
UNSPSC Code:
12352100
MDL number:
MFCD00456999

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InChI

1S/C8H6N2O3/c11-8-4-5-3-6(10(12)13)1-2-7(5)9-8/h1-3H,4H2,(H,9,11)

SMILES string

[O-][N+](=O)c1ccc2NC(=O)Cc2c1

InChI key

JQCGHRDKVZPCRO-UHFFFAOYSA-N

assay

97%

form

solid

mp

233-236 °C

Application

  • Reactant for synthesis of 3-[4-(amino/methylsulfonyl)phenyl]methylene-indolin-2-one derivatives as novel COX-1/2 and 5-LOX inhibitors
  • Reactant for preparation of Aurora kinase inhibitors
  • Reactant for synthesis of 3-substituted 2-indolinone RET inhibitors
  • Reactant for synthesis of 4-azachromeno[2,3-b]indol-11(6H)-ones and derivatives as analogs of ellipticine
  • Reactant for preparation of [18F]fluorobenzylidene-indolinone as possible tyrosine kinase inhibitor for PET tumor imaging
  • Reactant for preparation of 3-substituted indolin-2-ones as neuroprotective and toxic agents

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKBJ0281V
MKBB1654V
MKBB1654
01803HJ
08318TH

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Boris Letribot et al.
Molecules (Basel, Switzerland), 23(6) (2018-06-13)
Alkylidene oxindoles are important functional moieties and building blocks in pharmaceutical and synthetic chemistry. Our interest in biologically active compounds focused our studies on the synthesis of novel oxindoles, bearing on the exocyclic double bond at the C8, CN, and
Ayman M Saleh et al.
Molecules (Basel, Switzerland), 19(9), 13076-13092 (2014-08-27)
A selected set of substituted pyridone-annelated isoindigos 3a-f has been synthesized via interaction of 5- and 6-substituted oxindoles 2a-f with 6-ethyl-1,2,9-trioxopyrrolo[3,2-f]quinoline-8-carboxylic acid (1) in acetic acid at reflux. Among these isoindigos, the 5'-chloro and 5'-bromo derivatives 3b and 3d show

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