4-Aminoindole - ≥97% , CAS No.5192-23-4

CAS: 5192-23-4 Cat. No.: A115486 Peso molecular: 132.16 Beilstein Registry Number: 114919 Número EC: 621-202-0
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
GEO-00149 | MLS001148152 | 4-amino-1H-indol | FT-0617577 | SCHEMBL113992 | W-202957 | 4-amino-1h-indole | 1H-Indol-4-amine | 2P-050 | A828850 | 4-aminoindol | AKOS005206886 | A3574 | BBL100183 | DTXSID50342629 | B1202 | indol-4-ylamine | MFCD01076559 | Z9
Storage
Argon charged,Room temperature
Shipped In
Normal
Size
Estado
Price
Qty
250mg
A115486-250mg
3

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
1g
A115486-1g
4

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
5g
A115486-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

54,90US$

82,90US$
Guardar 28,00 US$ (33.78%)
25g
A115486-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

249,90US$

374,90US$
Guardar 125,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

4-Aminoindole is an indole derivative. Its cytokinin activity has been assessed by tobacco pith callus bioassay.4-Aminoindole can be prepared by reacting 2,6-dinitrotoluene and N,N-dimethylformamide dimethylacetal in anhydrous DMF.
Reactant for preparation of:

●Inhibitors of bacterial thymidylate synthase

●Mimetics of non-alkaloid toxin lignan anticancer and antiviral agent Podophyllotoxin (PPT)

●Inhibitors of Gli1-mediated transcription in the Hedgehog pathway

●Protein kinase C θ (PKCθ) inhibitors

●Indolic non-peptidic HIV protease inhibitors

●Transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonists

●Cyclooxygenase-2 (COX-2) and lipoxygenase (LOX) inhibitors

●11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) inhibitors

●Short chain 4-substituted indoles as potent αvβ3 antagonist

●Ligands of serotonin transporter and 5-HT1A receptors

Specifications

Sinónimos
GEO-00149 | MLS001148152 | 4-amino-1H-indol | FT-0617577 | SCHEMBL113992 | W-202957 | 4-amino-1h-indole | 1H-Indol-4-amine | 2P-050 | A828850 | 4-aminoindol | AKOS005206886 | A3574 | BBL100183 | DTXSID50342629 | B1202 | indol-4-ylamine | MFCD01076559 | Z9
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥97%
Nombres e identificadores
Pubchem Sid488190442
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488190442
Sonrisas canónicasC1=CC(=C2C=CNC2=C1)N
IUPAC Name1H-indol-4-amine
InChIKeyLUNUNJFSHKSXGQ-UHFFFAOYSA-N
INCHI1S/C8H8N2/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,9H2
Isómeros SMILES C1=CC(=C2C=CNC2=C1)N
WGK Alemania 3
Peso molecular 132.16
Beilstein 114919
Reaxy-Rn 114919
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114919&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
ClaseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct ParentIndoles
Alternative Parents Benzenoids  Pyrroles  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
I2117205Certificate of AnalysisJul 10, 2025 A115486
I2117206Certificate of AnalysisJul 10, 2025 A115486
I2117207Certificate of AnalysisJul 10, 2025 A115486
B2511088Certificate of AnalysisApr 13, 2024 A115486
C2027083Certificate of AnalysisJan 15, 2024 A115486
E2311306Certificate of AnalysisJun 25, 2021 A115486
Propiedades químicas y físicas
Sensibilidadair&light sensitive
Punto de fusión (°C)106-109°C
Peso molecular132.160 g/mol
XLogP32.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass132.069 Da
Monoisotopic Mass132.069 Da
Topological Polar Surface Area41.800 Ų
Heavy Atom Count10
Formal Charge0
Complexity124.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Xiaoqian Li, Xiaohua Jia, Jin Yang, Yong Li, Hongliang Lin, Haojie Song.  (2023)  Synergism of non-covalent interaction and ZIF-8@GO to improve tribological and mechanical properties of carbon fiber reinforced recyclable indole-based poly(hexahydrotriazine) composites.  POLYMER COMPOSITES,      [PMID:] [10.1002/pc.28049]
2. Ting-Ting Li, Qiang Wan, Xin Zhang, Yuan Xiao, Li-Ying Sun, Yu-Rong Zhang, Xiang-Nan Liu, Wan-Chao Yang.  (2022)  Stellate ganglion block reduces inflammation and improves neurological function in diabetic rats during ischemic stroke.  Neural Regeneration Research,      [PMID:35142688] [10.4103/1673-5374.335162]
Calculadoras de soluciones
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