5-Nitroisatin - ≥98%(HPLC) , CAS No.611-09-6

CAS: 611-09-6 Cat. No.: N136966 Fórmula: C8H4N2O4 Peso molecular: 192.13 Beilstein Registry Number: 21(3/4)5015 Número CE: 210-252-5
Disponível para encomenda
GRADE & PURITY ≥98%(HPLC)
Synonyms
NSC 525798 | 5-nitro-2,3-dihydro-1H-indole-2,3-dione | 5-Nitro-2,3-indolinedione | InChI=1/C8H4N2O4/c11-7-5-3-4(10(13)14)1-2-6(5)9-8(7)12/h1-3H,(H,9,11,12) | Q27281191 | CCRIS 4031 | Isatin-based compound, 37 | SY039358 | 5-Nitroindoline-2,3-dione | AC-50
Storage
Room temperature
Shipped In
Normal
★
Size
Alemanha (EU)
USA*
Price
Qty
1g
N136966-1g
—
5 Em stock
8,59€
5g
N136966-5g
—
Em stock ≥10
9,46€
10g
N136966-10g
Sob encomenda · 8–12 semanas

12,93€

19,87€
Gravar 6,94 € (34.93%)
25g
N136966-25g
—
4 Em stock

20,74€

31,15€
Gravar 10,41 € (33.43%)
100g
N136966-100g
—
3 Em stock

82,35€

124,00€
Gravar 41,65 € (33.59%)
500g
N136966-500g
1 Em stock
1 Em stock

393,87€

590,84€
Gravar 196,98 € (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

5-Nitroisatin is a useful reactant for the synthesis of antibacterial, antifungal, antimycobacterial, antimicrobial, ans antitubercular agents. 5-Nitroisatin is also used to synthesize spiro[indole-thiazolidinones], anticonvulsant agents, human transglutaminase 2 inhibitors, anthelmic agents, acetylcholinesterase inhibitors, and anti-HIV agents.

Specifications

Sinónimos
NSC 525798 | 5-nitro-2,3-dihydro-1H-indole-2,3-dione | 5-Nitro-2,3-indolinedione | InChI=1/C8H4N2O4/c11-7-5-3-4(10(13)14)1-2-6(5)9-8(7)12/h1-3H,(H,9,11,12) | Q27281191 | CCRIS 4031 | Isatin-based compound, 37 | SY039358 | 5-Nitroindoline-2,3-dione | AC-50
Especificações e pureza
≥98%(HPLC)
Condições de armazenamento de armazenamento
Room temperature
Enviado em
Normal
Pureza
≥98%(HPLC)
Nomes e identificadores
Pubchem Sid488194954
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488194954
Sorrisos canónicosC1=CC2=C(C=C1[N+](=O)[O-])C(=O)C(=O)N2
IUPAC Name5-nitro-1H-indole-2,3-dione
InChIKeyUNMYHYODJHKLOC-UHFFFAOYSA-N
INCHI1S/C8H4N2O4/c11-7-5-3-4(10(13)14)1-2-6(5)9-8(7)12/h1-3H,(H,9,11,12)
SMILES isoméricas C1=CC2=C(C=C1[N+](=O)[O-])C(=O)C(=O)N2
WGK Alemanha 3
RTECS NL7970000
Peso molecular 192.13
Beilstein 21(3/4)5015
Reaxy-Rn 180223
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=180223&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseIndoles and derivatives
SubclassIndolines
Intermediate Tree Nodes Not available
Direct ParentIndolines
Alternative Parents Nitroaromatic compounds  Aryl ketones  Benzenoids  Vinylogous amides  Secondary carboxylic acid amides  Lactams  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Dihydroindole - Nitroaromatic compound - Aryl ketone - Benzenoid - Vinylogous amide - Carboxamide group - Ketone - Lactam - C-nitro compound - Secondary carboxylic acid amide - Organic nitro compound - Carboxylic acid derivative - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Aromatic heteropolycyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as indolines. These are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
CASP3 Tchem Caspase-3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP3 Tchem Caspase-3 (3632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CES1 Tchem Acyl coenzyme A:cholesterol acyltransferase (1029 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-937 (7138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SW-620 (52400 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ASPC1 (1310 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alvos associados (não humanos)
Cruzipain (33337 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALS Acetolactate synthase (354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pfmrk Protein kinase Pfmrk (149 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Falcipain 2 (539 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brassica rapa subsp. oleifera (1696 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDataItem
F1529099Certificate of AnalysisJul 07, 2026 N136966
E2217132Certificate of AnalysisDec 12, 2025 N136966
E2217155Certificate of AnalysisDec 12, 2025 N136966
E2217156Certificate of AnalysisDec 12, 2025 N136966
K2503118Certificate of AnalysisNov 17, 2025 N136966
A2226076Certificate of AnalysisAug 11, 2025 N136966
D2323541Certificate of AnalysisFeb 11, 2025 N136966
Propriedades químicas e físicas
SolubilidadeSolubility in N,N-DMF very faint turbidity
Ponto de fusão (°C)251 °C
Peso molecular192.130 g/mol
XLogP30.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass192.017 Da
Monoisotopic Mass192.017 Da
Topological Polar Surface Area92.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity309.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluções
Revisões

Avaliações dos Clientes

Perguntas frequentes

What is the purity of this product, and how is it determined?
This product is supplied at ≥98% purity, determined by HPLC. Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at room temperature.
How is this product shipped?
This product ships under standard ambient conditions. No temperature-controlled packaging is required.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 611-09-6, the molecular formula is C8H4N2O4, and the molecular weight is 192.13 g/mol. InChIKey UNMYHYODJHKLOC-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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