HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 11831752Erstellt: 31. Oktober 2026
1-BOC-5-methoxyindole
N-BOC-5-METHOXYINDOLE · 1-Boc-5-methoxyindole · 1-Boc-5-methoxy-1H-indole · 5-Methoxy-1H-indole, N-BOC protected · 5-Methoxy-1H-indole,N-BOCprotected98% · N-(tert-Butoxycarbonyl)-5-methoxyindole · 5-Methoxy-1H-indole, N-BOC protected 98% · tert-butyl 5-methoxyindole-1-carboxylate
https://huagongshe.com/de/chemical/11831752
Identifikatoren & physikalische Daten
| CAS No. | 99275-47-5 |
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| Summenformel | C14H17NO3 |
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| Durchschnittliche Molmasse | 247,294 g/mol |
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| Monoisotopische Masse | 247,1208434 g/mol |
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| SMILES | COc1ccc2c(ccn2C(=O)OC(C)(C)C)c1 |
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| InChIKey | LPSLGTZFBDZNEK-UHFFFAOYSA-N |
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| PubChem CID | 11831752 |
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| EC No. | 624-821-4 |
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| DTXSID | DTXSID00474161 |
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Chemische & physikalische Eigenschaften
| Schmelzpunkt | 75-79 °C |
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| Siedepunkt | 357.3±34.0 °C(Predicted) |
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| Dichte | 1.10±0.1 g/cm3(Predicted) |
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| Lagerbedingungen | Inert atmosphere,2-8°C |
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| Aggregatzustand | solid |
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| InChI | InChI=1S/C14H17NO3/c1-14(2,3)18-13(16)15-8-7-10-9-11(17-4)5-6-12(10)15/h5-9H,1-4H3 |
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| InChIKey | LPSLGTZFBDZNEK-UHFFFAOYSA-N |
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| SMILES | N1(C(OC(C)(C)C)=O)C2=C(C=C(OC)C=C2)C=C1 |
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| CAS Datenbank | 99275-47-5(CAS DataBase Reference) |
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Sicherheit & Vorschriften
| Wassergefährdungsklasse (WGK) | 3 |
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| UN-Transportnummer | UN 2811 6.1/PG 3 |
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| R-Sätze (R) | 22-36 |
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| Gefahrensymbole | Xi,Xn |
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| hazard_note | Harmful/Irritant/Keep Cold |
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| Sicherheitshinweise (S) | 26 |
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| Lagerklasse | 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects |
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| Gefahrenklasse | Acute Tox. 3 OralEye Irrit. 2 |
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Anwendungen & Verwendung
Verwenden
Reactant for preparation of:• ;Asymmetric intramolecular Friedel-Crafts alkylation reaction1• ;Palladium-catalyzed carboaminoxylations with arylboronic acids and TEMPO catalyst2• ;Fluorescent pyrimidopyrimidoindole nucleosides via Suzuki-Miyaura coupling reaction3• ;Novel conformationally restricted β- and γ-amino acids4• ;2-(Indolyl) borates, silanes, and silanols5• ;DNA minor groove alkylating agents as stable amine-based prodrugs designed for tumor-specific release6
