YH 239-EE - ≥98%(HPLC) , CAS No.1364488-67-4

CAS: 1364488-67-4 Cat. No.: Y287733 Summenformel: C25H27Cl2N3O4 Molekulargewicht: 504.41 PubChem CID: 56943013
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GRADE & PURITY ≥98%(HPLC)
Synonyms
Ethyl-3-[2-(tert.-Butylamino)-1-[N-(4-Chlorbenzyl)formamido]-2-oxoethyl]-6-chlor-1H-indol-2-carboxylat
Storage
Lagerung bei -20°C
Shipped In
Eistruhe + Eispads
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Size
Deutschland (EU)
USA*
Price
Qty
5mg
Y287733-5mg
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2 Auf Lager

45,04€

67,60€
Speichern 22,56 € (33.38%)
10mg
Y287733-10mg
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2 Auf Lager

79,75€

119,66€
Speichern 39,92 € (33.36%)
25mg
Y287733-25mg
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2 Auf Lager

175,20€

262,84€
Speichern 87,64 € (33.34%)
50mg
Y287733-50mg
Auf Bestellung · 8–12 Wochen

214,24€

321,84€
Speichern 107,60 € (33.43%)
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Why this grade

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

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Storage & shipping

Lagerung bei -20°C Ships Eistruhe + Eispads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

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

Specifications

Synonyme
Ethyl-3-[2-(tert.-Butylamino)-1-[N-(4-Chlorbenzyl)formamido]-2-oxoethyl]-6-chlor-1H-indol-2-carboxylat
Spezifikationen & Reinheit
≥98%(HPLC)
Biochemische und physiologische Mechanismen
MDM2-Hemmstoff. Unterbricht MDM2-p53 und aktiviert die p53-Aktivität in vitro. Verhindert die mitotische Katastrophe und fördert das Überleben von gealterten Muskelstammzellen (muSCs). Hemmt auch die Proliferation von AML-Zellen in vitro.
Storage
Lagerung bei -20°C
Verschickt in
Eistruhe + Eispads
Reinheit
≥98%(HPLC)
Namen und Kennungen
Pubchem Sid504771495
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504771495
Kanonisches LächelnCCOC(=O)C1=C(C2=C(N1)C=C(C=C2)Cl)C(C(=O)NC(C)(C)C)N(CC3=CC=C(C=C3)Cl)C=O
IUPAC Nameethyl 3-[2-(tert-butylamino)-1-[(4-chlorophenyl)methyl-formylamino]-2-oxoethyl]-6-chloro-1H-indole-2-carboxylate
InChIKeyOTUBDDRFPQLPKD-UHFFFAOYSA-N
INCHI1S/C25H27Cl2N3O4/c1-5-34-24(33)21-20(18-11-10-17(27)12-19(18)28-21)22(23(32)29-25(2,3)4)30(14-31)13-15-6-8-16(26)9-7-15/h6-12,14,22,28H,5,13H2,1-4H3,(H,29,32)
Isomere SMILES CCOC(=O)C1=C(C2=C(N1)C=C(C=C2)Cl)C(C(=O)NC(C)(C)C)N(CC3=CC=C(C=C3)Cl)C=O
PubChem CID 56943013
Molekulargewicht 504.41

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.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlasseIndoles and derivatives
SubclassIndolecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndolecarboxylic acids and derivatives
Alternative Parents 3-alkylindoles  Alpha amino acids and derivatives  Pyrrole carboxylic acids and derivatives  Chlorobenzenes  Substituted pyrroles  Aryl chlorides  Tertiary carboxylic acid amides  Heteroaromatic compounds  Secondary carboxylic acid amides  Carboxylic acid esters  Azacyclic compounds  Carbonyl compounds  Hydrocarbon derivatives  Organic oxides  Organochlorides  Organonitrogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indolecarboxylic acid derivative - Alpha-amino acid or derivatives - 3-alkylindole - Indole - Pyrrole-2-carboxylic acid or derivatives - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Tertiary carboxylic acid amide - Pyrrole - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxamide group - Azacycle - Carboxylic acid derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organochloride - Organohalogen compound - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as indolecarboxylic acids and derivatives. These are compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

4 results found

Lot NumberCertificate TypeDatumArtikel
G2220121Certificate of AnalysisMay 09, 2025 Y287733
G2220122Certificate of AnalysisMay 09, 2025 Y287733
G2220127Certificate of AnalysisMay 09, 2025 Y287733
G2220128Certificate of AnalysisMay 09, 2025 Y287733
Chemische und physikalische Eigenschaften
LöslichkeitSolvent:DMSO, Max Conc. mg/mL: 50.44, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 10.09, Max Conc. mM: 20
Molekulargewicht504.400 g/mol
XLogP35.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count9
Exact Mass503.138 Da
Monoisotopic Mass503.138 Da
Topological Polar Surface Area91.500 Ų
Heavy Atom Count34
Formal Charge0
Complexity723.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Lösungsrechner
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