Pyrrolidine,1-(2,4-dinitrophenyl)

Modify Date: 2025-08-27 16:41:18

Pyrrolidine,1-(2,4-dinitrophenyl) Structure
Pyrrolidine,1-(2,4-dinitrophenyl) structure
Common Name Pyrrolidine,1-(2,4-dinitrophenyl)
CAS Number 14552-00-2 Molecular Weight 237.21200
Density 1.414g/cm3 Boiling Point 408.6ºC at 760mmHg
Molecular Formula C10H11N3O4 Melting Point N/A
MSDS N/A Flash Point 200.9ºC

 Names

Name 1-(2,4-dinitrophenyl)pyrrolidine
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.414g/cm3
Boiling Point 408.6ºC at 760mmHg
Molecular Formula C10H11N3O4
Molecular Weight 237.21200
Flash Point 200.9ºC
Exact Mass 237.07500
PSA 94.88000
LogP 3.21460
Vapour Pressure 6.94E-07mmHg at 25°C
Index of Refraction 1.628
InChIKey ARCUVLVHQWONDY-UHFFFAOYSA-N
SMILES O=[N+]([O-])c1ccc(N2CCCC2)c([N+](=O)[O-])c1

 Safety Information

HS Code 2933990090

 Synthetic Route

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Pyrrolidine,1-(2,4-dinitrophenyl)Bioassay

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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1100
Name: qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
Source: NCGC
Target: TDP1 protein [Homo sapiens]
External Id: TDP1101
Name: Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
Source: Broad Institute
Target: N/A
External Id: 2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
Name: qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
Source: NCGC
Target: apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id: AMA1100
Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id: ABHD4_INH_FP_1536_1X%INH PRUN
Name: High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
Source: Southern Research Institute
Target: HIV-1 Vif
External Id: HIV1-VIF_MS
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 Synonyms

1-Pyrrolidino-2,4-dinitrobenzene
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