tert-Butyl 1H-indol-4-ylcarbamate
Based on 1 Customer Validation
tert-Butyl 1H-indol-4-ylcarbamate is a nucleophilic reagent. tert-Butyl 1H-indol-4-ylcarbamate induces the formation of the stable triple hydrogen-bonded complex A-TS-Re. tert-Butyl 1H-indol-4-ylcarbamate undergoes Friedel-Crafts reactions with β,γ-unsaturated α-ketiminoesters.
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- CAS No.: 819850-13-0
- Formula: C13H16N2O2
- Molecular Weight:232.28
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Biological Activity
Description
In Vitro
tert-Butyl 1H-indol-4-ylcarbamate induces the formation of a stable triple hydrogen-bonded complex A-TS-Re. tert-Butyl 1H-indol-4-ylcarbamate undergoes Friedel-Crafts reactions with β,γ-unsaturated α-ketiminoesters[1][2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 819850-13-0
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Appearance Solid
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Molecular Weight 232.28
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Formula C13H16N2O2
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Color Off-white to light brown
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SMILES
CC(C)(OC(NC1=CC=CC2=C1C=CN2)=O)C
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Purity & Documentation
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Data Sheet (271 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- tert-Butyl 1H-indol-4-ylcarbamate
- 819850-13-0
- Biochemical Assay Reagents
- Friedel-Crafts alkylation
- Friedel-Crafts reactions
- enantioselectivity
- chiral phosphoric acid
- C3-functionalized indole
- β,γ-unsaturated α-ketiminoesters
- transition state complex
- 2-furyl
- 1H-indol-4-ylcarbamate
- 2-thienyl
- Inhibitor
- inhibitor
- inhibit